Canonical Allele Identifier: CA2063464638

Gene: ALDH2

Linked Data

• dbSNP Id: rs2068506686

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111807547A>T , CM000674.2:g.111807547A>T	GRCh38
NC_000012.11:g.112245351A>T , CM000674.1:g.112245351A>T	GRCh37
NC_000012.10:g.110729734A>T	NCBI36
NG_012250.1:g.46006A>T
NG_012250.2:g.45661A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261733.7:c.1522-1996A>T MANE Select	ENSP00000261733.2:n.1522-1996A>T
ENST00000261733.6:c.1522-1996A>T	ENSP00000261733.2:n.1522-1996A>T
ENST00000416293.7:c.1381-1996A>T	ENSP00000403349.3:n.1381-1996A>T
ENST00000548536.1:c.*1398-1996A>T	ENSP00000448179.1:n.*1398-1996A>T
ENST00000549106.1:c.453-1996A>T
NM_000690.3:c.1522-1996A>T	NP_000681.2:n.1522-1996A>T
NM_001204889.1:c.1381-1996A>T	NP_001191818.1:n.1381-1996A>T
NM_000690.4:c.1522-1996A>T MANE Select	NP_000681.2:n.1522-1996A>T
NM_001204889.2:c.1381-1996A>T	NP_001191818.1:n.1381-1996A>T