Canonical Allele Identifier: CA2063449985
Gene: ALDH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111791125G= , CM000674.2:g.111791125G= GRCh38
NC_000012.11:g.112228929G= , CM000674.1:g.112228929G= GRCh37
NC_000012.10:g.110713312G= NCBI36
NG_012250.1:g.29584G=
NG_012250.2:g.29239G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.682-181G= MANE Select ENSP00000261733.2:n.682-181G=
ENST00000546840.3:c.672-181G=
ENST00000261733.6:c.682-181G= ENSP00000261733.2:n.682-181G=
ENST00000416293.7:c.541-181G= ENSP00000403349.3:n.541-181G=
ENST00000546840.2:c.667-181G= ENSP00000450353.3:n.667-181G=
ENST00000548536.1:c.*558-181G= ENSP00000448179.1:n.*558-181G=
NM_000690.3:c.682-181G= NP_000681.2:n.682-181G=
NM_001204889.1:c.541-181G= NP_001191818.1:n.541-181G=
NM_000690.4:c.682-181G= MANE Select NP_000681.2:n.682-181G=
NM_001204889.2:c.541-181G= NP_001191818.1:n.541-181G=
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