Canonical Allele Identifier: CA2063442950

Gene: ALDH2

Linked Data

• dbSNP Id: rs1319291681

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111776586G>C , CM000674.2:g.111776586G>C	GRCh38
NC_000012.11:g.112214390G>C , CM000674.1:g.112214390G>C	GRCh37
NC_000012.10:g.110698773G>C	NCBI36
NG_012250.1:g.15045G>C
NG_012250.2:g.14700G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261733.7:c.115-5332G>C MANE Select	ENSP00000261733.2:n.115-5332G>C
ENST00000546840.3:c.105-5332G>C
ENST00000261733.6:c.115-5332G>C	ENSP00000261733.2:n.115-5332G>C
ENST00000416293.7:c.115-5332G>C	ENSP00000403349.3:n.115-5332G>C
ENST00000546840.2:c.100-5332G>C	ENSP00000450353.3:n.100-5332G>C
ENST00000548536.1:c.230+866G>C	ENSP00000448179.1:n.230+866G>C
NM_000690.3:c.115-5332G>C	NP_000681.2:n.115-5332G>C
NM_001204889.1:c.115-5332G>C	NP_001191818.1:n.115-5332G>C
NM_000690.4:c.115-5332G>C MANE Select	NP_000681.2:n.115-5332G>C
NM_001204889.2:c.115-5332G>C	NP_001191818.1:n.115-5332G>C