Canonical Allele Identifier: CA2554812379
Gene: ALDH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111791067C>A , CM000674.2:g.111791067C>A GRCh38
NC_000012.11:g.112228871C>A , CM000674.1:g.112228871C>A GRCh37
NC_000012.10:g.110713254C>A NCBI36
NG_012250.1:g.29526C>A
NG_012250.2:g.29181C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.682-239C>A MANE Select ENSP00000261733.2:n.682-239C>A
ENST00000546840.3:c.672-239C>A
ENST00000261733.6:c.682-239C>A ENSP00000261733.2:n.682-239C>A
ENST00000416293.7:c.541-239C>A ENSP00000403349.3:n.541-239C>A
ENST00000546840.2:c.667-239C>A ENSP00000450353.3:n.667-239C>A
ENST00000548536.1:c.*558-239C>A ENSP00000448179.1:n.*558-239C>A
NM_000690.3:c.682-239C>A NP_000681.2:n.682-239C>A
NM_001204889.1:c.541-239C>A NP_001191818.1:n.541-239C>A
NM_000690.4:c.682-239C>A MANE Select NP_000681.2:n.682-239C>A
NM_001204889.2:c.541-239C>A NP_001191818.1:n.541-239C>A
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