Canonical Allele Identifier: CA2063441681

Gene: ALDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111774029T= , CM000674.2:g.111774029T=	GRCh38
NC_000012.11:g.112211833T= , CM000674.1:g.112211833T=	GRCh37
NC_000012.10:g.110696216T=	NCBI36
NG_012250.1:g.12488T=
NG_012250.2:g.12143T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000690.4:c.114+6933T= MANE Select	NP_000681.2:n.114+6933T=
ENST00000261733.7:c.114+6933T= MANE Select	ENSP00000261733.2:n.114+6933T=
NM_000690.3:c.114+6933T=	NP_000681.2:n.114+6933T=
NM_001204889.1:c.114+6933T=	NP_001191818.1:n.114+6933T=
NM_001204889.2:c.114+6933T=	NP_001191818.1:n.114+6933T=
ENST00000261733.6:c.114+6933T=	ENSP00000261733.2:n.114+6933T=
ENST00000416293.7:c.114+6933T=	ENSP00000403349.3:n.114+6933T=
ENST00000546840.2:c.100-7889T=	ENSP00000450353.3:n.100-7889T=
ENST00000546840.3:c.105-7889T=
ENST00000548536.1:c.115-1576T=	ENSP00000448179.1:n.115-1576T=