Canonical Allele Identifier: CA357497372
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs764699940
gnomAD v3: 4-99420546-T-A
gnomAD v4: 4-99420546-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420546T>A , CM000666.2:g.99420546T>A GRCh38
NC_000004.11:g.100341703T>A , CM000666.1:g.100341703T>A GRCh37
NC_000004.10:g.100560726T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.812A>T MANE Select ENSP00000414254.2:p.His271Leu
ENST00000209665.8:c.848A>T ENSP00000209665.4:p.His283Leu
ENST00000437033.6:c.812A>T ENSP00000414254.2:p.His271Leu
ENST00000476959.5:c.872A>T ENSP00000420269.1:p.His291Leu
ENST00000482593.5:c.641A>T ENSP00000420613.1:p.His214Leu
NM_000673.4:c.848A>T NP_000664.2:p.His283Leu
NM_001166504.1:c.872A>T NP_001159976.1:p.His291Leu
NM_000673.7:c.812A>T MANE Select NP_000664.3:p.His271Leu
NM_001166504.2:c.872A>T NP_001159976.1:p.His291Leu