Canonical Allele Identifier: CA481775796
Gene: ALDH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.112241687A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111803883A>C , CM000674.2:g.111803883A>C GRCh38
NC_000012.11:g.112241687A>C , CM000674.1:g.112241687A>C GRCh37
NC_000012.10:g.110726070A>C NCBI36
NG_012250.1:g.42342A>C
NG_012250.2:g.41997A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1431A>C MANE Select ENSP00000261733.2:p.Gly477=
ENST00000261733.6:c.1431A>C ENSP00000261733.2:p.Gly477=
ENST00000416293.7:c.1290A>C ENSP00000403349.3:p.Gly430=
ENST00000548536.1:c.*1307A>C ENSP00000448179.1:n.*1307A>C
ENST00000549106.1:c.362A>C
NM_000690.3:c.1431A>C NP_000681.2:p.Gly477=
NM_001204889.1:c.1290A>C NP_001191818.1:p.Gly430=
NM_000690.4:c.1431A>C MANE Select NP_000681.2:p.Gly477=
NM_001204889.2:c.1290A>C NP_001191818.1:p.Gly430=