Canonical Allele Identifier: CA951862842
Gene: ALDH2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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