Canonical Allele Identifier: CA243665676
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs928853857

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111807874A>G , CM000674.2:g.111807874A>G GRCh38
NC_000012.11:g.112245678A>G , CM000674.1:g.112245678A>G GRCh37
NC_000012.10:g.110730061A>G NCBI36
NG_012250.1:g.46333A>G
NG_012250.2:g.45988A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.1522-1669A>G MANE Select ENSP00000261733.2:n.1522-1669A>G
ENST00000261733.6:c.1522-1669A>G ENSP00000261733.2:n.1522-1669A>G
ENST00000416293.7:c.1381-1669A>G ENSP00000403349.3:n.1381-1669A>G
ENST00000548536.1:c.*1398-1669A>G ENSP00000448179.1:n.*1398-1669A>G
ENST00000549106.1:c.453-1669A>G
NM_000690.3:c.1522-1669A>G NP_000681.2:n.1522-1669A>G
NM_001204889.1:c.1381-1669A>G NP_001191818.1:n.1381-1669A>G
NM_000690.4:c.1522-1669A>G MANE Select NP_000681.2:n.1522-1669A>G
NM_001204889.2:c.1381-1669A>G NP_001191818.1:n.1381-1669A>G