Canonical Allele Identifier: CA2063442949
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2068236920

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776579G>T , CM000674.2:g.111776579G>T GRCh38
NC_000012.11:g.112214383G>T , CM000674.1:g.112214383G>T GRCh37
NC_000012.10:g.110698766G>T NCBI36
NG_012250.1:g.15038G>T
NG_012250.2:g.14693G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5339G>T MANE Select ENSP00000261733.2:n.115-5339G>T
ENST00000546840.3:c.105-5339G>T
ENST00000261733.6:c.115-5339G>T ENSP00000261733.2:n.115-5339G>T
ENST00000416293.7:c.115-5339G>T ENSP00000403349.3:n.115-5339G>T
ENST00000546840.2:c.100-5339G>T ENSP00000450353.3:n.100-5339G>T
ENST00000548536.1:c.230+859G>T ENSP00000448179.1:n.230+859G>T
NM_000690.3:c.115-5339G>T NP_000681.2:n.115-5339G>T
NM_001204889.1:c.115-5339G>T NP_001191818.1:n.115-5339G>T
NM_000690.4:c.115-5339G>T MANE Select NP_000681.2:n.115-5339G>T
NM_001204889.2:c.115-5339G>T NP_001191818.1:n.115-5339G>T