Canonical Allele Identifier: CA951863102
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2068237410

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776671G>A , CM000674.2:g.111776671G>A GRCh38
NC_000012.11:g.112214475G>A , CM000674.1:g.112214475G>A GRCh37
NC_000012.10:g.110698858G>A NCBI36
NG_012250.1:g.15130G>A
NG_012250.2:g.14785G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5247G>A MANE Select ENSP00000261733.2:n.115-5247G>A
ENST00000546840.3:c.105-5247G>A
ENST00000261733.6:c.115-5247G>A ENSP00000261733.2:n.115-5247G>A
ENST00000416293.7:c.115-5247G>A ENSP00000403349.3:n.115-5247G>A
ENST00000546840.2:c.100-5247G>A ENSP00000450353.3:n.100-5247G>A
ENST00000548536.1:c.230+951G>A ENSP00000448179.1:n.230+951G>A
NM_000690.3:c.115-5247G>A NP_000681.2:n.115-5247G>A
NM_001204889.1:c.115-5247G>A NP_001191818.1:n.115-5247G>A
NM_000690.4:c.115-5247G>A MANE Select NP_000681.2:n.115-5247G>A
NM_001204889.2:c.115-5247G>A NP_001191818.1:n.115-5247G>A