Canonical Allele Identifier: CA2063442997
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2068237663
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776713del , CM000674.2:g.111776713del GRCh38
NC_000012.11:g.112214517del , CM000674.1:g.112214517del GRCh37
NC_000012.10:g.110698900del NCBI36
NG_012250.1:g.15172del
NG_012250.2:g.14827del

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5205del MANE Select ENSP00000261733.2:n.115-5205del
ENST00000546840.3:c.105-5205del
ENST00000261733.6:c.115-5205del ENSP00000261733.2:n.115-5205del
ENST00000416293.7:c.115-5205del ENSP00000403349.3:n.115-5205del
ENST00000546840.2:c.100-5205del ENSP00000450353.3:n.100-5205del
ENST00000548536.1:c.230+993del ENSP00000448179.1:n.230+993del
NM_000690.3:c.115-5205del NP_000681.2:n.115-5205del
NM_001204889.1:c.115-5205del NP_001191818.1:n.115-5205del
NM_000690.4:c.115-5205del MANE Select NP_000681.2:n.115-5205del
NM_001204889.2:c.115-5205del NP_001191818.1:n.115-5205del
Search 100 bp 5'
Search 100 bp 3'