Canonical Allele Identifier: CA2797478726
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776472A>G , CM000674.2:g.111776472A>G GRCh38
NC_000012.11:g.112214276A>G , CM000674.1:g.112214276A>G GRCh37
NC_000012.10:g.110698659A>G NCBI36
NG_012250.1:g.14931A>G
NG_012250.2:g.14586A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.115-5446A>G MANE Select ENSP00000261733.2:n.115-5446A>G
ENST00000546840.3:c.105-5446A>G
ENST00000261733.6:c.115-5446A>G ENSP00000261733.2:n.115-5446A>G
ENST00000416293.7:c.115-5446A>G ENSP00000403349.3:n.115-5446A>G
ENST00000546840.2:c.100-5446A>G ENSP00000450353.3:n.100-5446A>G
ENST00000548536.1:c.230+752A>G ENSP00000448179.1:n.230+752A>G
NM_000690.3:c.115-5446A>G NP_000681.2:n.115-5446A>G
NM_001204889.1:c.115-5446A>G NP_001191818.1:n.115-5446A>G
NM_000690.4:c.115-5446A>G MANE Select NP_000681.2:n.115-5446A>G
NM_001204889.2:c.115-5446A>G NP_001191818.1:n.115-5446A>G