Canonical Allele Identifier: CA5674757
Gene: CALHM1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2986017

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458495A>G , CM000672.2:g.103458495A>G GRCh38
NC_000010.9:g.105208242A>G NCBI36
NC_000010.10:g.105218252A>G , CM000672.1:g.105218252A>G GRCh37
NG_016855.1:g.5397T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.5:c.257T>C ENSP00000329926.5:p.Leu86Pro
NM_001001412.3:c.257T>C VV NP_001001412.3:p.Leu86Pro