Canonical Allele Identifier: CA2063442993
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2068237610
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776709T>G , CM000674.2:g.111776709T>G GRCh38
NC_000012.11:g.112214513T>G , CM000674.1:g.112214513T>G GRCh37
NC_000012.10:g.110698896T>G NCBI36
NG_012250.1:g.15168T>G
NG_012250.2:g.14823T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5209T>G MANE Select ENSP00000261733.2:n.115-5209T>G
ENST00000546840.3:c.105-5209T>G
ENST00000261733.6:c.115-5209T>G ENSP00000261733.2:n.115-5209T>G
ENST00000416293.7:c.115-5209T>G ENSP00000403349.3:n.115-5209T>G
ENST00000546840.2:c.100-5209T>G ENSP00000450353.3:n.100-5209T>G
ENST00000548536.1:c.230+989T>G ENSP00000448179.1:n.230+989T>G
NM_000690.3:c.115-5209T>G NP_000681.2:n.115-5209T>G
NM_001204889.1:c.115-5209T>G NP_001191818.1:n.115-5209T>G
NM_000690.4:c.115-5209T>G MANE Select NP_000681.2:n.115-5209T>G
NM_001204889.2:c.115-5209T>G NP_001191818.1:n.115-5209T>G
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