Canonical Allele Identifier: CA2063463752
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs1851370830

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111806440A>G , CM000674.2:g.111806440A>G GRCh38
NC_000012.11:g.112244244A>G , CM000674.1:g.112244244A>G GRCh37
NC_000012.10:g.110728627A>G NCBI36
NG_012250.1:g.44899A>G
NG_012250.2:g.44554A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1521+2467A>G MANE Select ENSP00000261733.2:n.1521+2467A>G
ENST00000261733.6:c.1521+2467A>G ENSP00000261733.2:n.1521+2467A>G
ENST00000416293.7:c.1380+2467A>G ENSP00000403349.3:n.1380+2467A>G
ENST00000548536.1:c.*1397+2467A>G ENSP00000448179.1:n.*1397+2467A>G
ENST00000549106.1:c.452+2467A>G
NM_000690.3:c.1521+2467A>G NP_000681.2:n.1521+2467A>G
NM_001204889.1:c.1380+2467A>G NP_001191818.1:n.1380+2467A>G
NM_000690.4:c.1521+2467A>G MANE Select NP_000681.2:n.1521+2467A>G
NM_001204889.2:c.1380+2467A>G NP_001191818.1:n.1380+2467A>G