rs112634214 Rat Genome Database

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Variant: rs112634214 -  Homo sapiens

RGD ID: 14725391
RS ID: rs112634214
ClinVar ID: CV671074
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALAS2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 55,042,349
GRCh38 X 55,015,916
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000032.5:c.1004-174G>A
NM_001037967.4:c.893-174G>A
NM_001037968.4:c.965-174G>A
NG_008983.1:g.20149G>A
More... 		06/19/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ALAS2
Accession:NM_000032
Location:INTRON

Gene Symbol:ALAS2
Accession:NM_001037968
Location:INTRON

Gene Symbol:ALAS2
Accession:NM_001037967
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000833419 CLINVAR
dbSNP (RS) rs112634214 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ALAS2 CLINVAR
OMIM 301300 CLINVAR