Canonical Allele Identifier: CA481775801
Gene: ALDH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.112241690C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111803886C>T , CM000674.2:g.111803886C>T GRCh38
NC_000012.11:g.112241690C>T , CM000674.1:g.112241690C>T GRCh37
NC_000012.10:g.110726073C>T NCBI36
NG_012250.1:g.42345C>T
NG_012250.2:g.42000C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1434C>T MANE Select ENSP00000261733.2:p.Ala478=
ENST00000261733.6:c.1434C>T ENSP00000261733.2:p.Ala478=
ENST00000416293.7:c.1293C>T ENSP00000403349.3:p.Ala431=
ENST00000548536.1:c.*1310C>T ENSP00000448179.1:n.*1310C>T
ENST00000549106.1:c.365C>T
NM_000690.3:c.1434C>T NP_000681.2:p.Ala478=
NM_001204889.1:c.1293C>T NP_001191818.1:p.Ala431=
NM_000690.4:c.1434C>T MANE Select NP_000681.2:p.Ala478=
NM_001204889.2:c.1293C>T NP_001191818.1:p.Ala431=