Canonical Allele Identifier: CA2063463760
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111806444A= , CM000674.2:g.111806444A= GRCh38
NC_000012.11:g.112244248A= , CM000674.1:g.112244248A= GRCh37
NC_000012.10:g.110728631A= NCBI36
NG_012250.1:g.44903A=
NG_012250.2:g.44558A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1521+2471A= MANE Select ENSP00000261733.2:n.1521+2471A=
ENST00000261733.6:c.1521+2471A= ENSP00000261733.2:n.1521+2471A=
ENST00000416293.7:c.1380+2471A= ENSP00000403349.3:n.1380+2471A=
ENST00000548536.1:c.*1397+2471A= ENSP00000448179.1:n.*1397+2471A=
ENST00000549106.1:c.452+2471A=
NM_000690.3:c.1521+2471A= NP_000681.2:n.1521+2471A=
NM_001204889.1:c.1380+2471A= NP_001191818.1:n.1380+2471A=
NM_000690.4:c.1521+2471A= MANE Select NP_000681.2:n.1521+2471A=
NM_001204889.2:c.1380+2471A= NP_001191818.1:n.1380+2471A=