Canonical Allele Identifier: CA13632884
Gene: ALDH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16941667

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111806609C>T , CM000674.2:g.111806609C>T GRCh38
NC_000012.10:g.110728796C>T NCBI36
NC_000012.11:g.112244413C>T , CM000674.1:g.112244413C>T GRCh37
NG_012250.1:g.45068C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.6:c.1521+2636C>T ENSP00000261733.2:p.=
ENST00000416293.7:c.1380+2636C>T ENSP00000403349.3:p.=
ENST00000548536.1:c.*1397+2636C>T ENSP00000448179.1:p.=
ENST00000549106.1:n.452+2636C>T
NM_000690.3:c.1521+2636C>T VV NP_000681.2:p.=
NM_001204889.1:c.1380+2636C>T VV NP_001191818.1:p.=