Canonical Allele Identifier: CA2063442979
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776668G= , CM000674.2:g.111776668G= GRCh38
NC_000012.11:g.112214472G= , CM000674.1:g.112214472G= GRCh37
NC_000012.10:g.110698855G= NCBI36
NG_012250.1:g.15127G=
NG_012250.2:g.14782G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5250G= MANE Select ENSP00000261733.2:n.115-5250G=
ENST00000546840.3:c.105-5250G=
ENST00000261733.6:c.115-5250G= ENSP00000261733.2:n.115-5250G=
ENST00000416293.7:c.115-5250G= ENSP00000403349.3:n.115-5250G=
ENST00000546840.2:c.100-5250G= ENSP00000450353.3:n.100-5250G=
ENST00000548536.1:c.230+948G= ENSP00000448179.1:n.230+948G=
NM_000690.3:c.115-5250G= NP_000681.2:n.115-5250G=
NM_001204889.1:c.115-5250G= NP_001191818.1:n.115-5250G=
NM_000690.4:c.115-5250G= MANE Select NP_000681.2:n.115-5250G=
NM_001204889.2:c.115-5250G= NP_001191818.1:n.115-5250G=