Canonical Allele Identifier: CA102646227
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs761122139

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420751C>T , CM000666.2:g.99420751C>T GRCh38
NC_000004.11:g.100341908C>T , CM000666.1:g.100341908C>T GRCh37
NC_000004.10:g.100560931C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.607G>A MANE Select ENSP00000414254.2:p.Val203Ile
ENST00000209665.8:c.643G>A ENSP00000209665.4:p.Val215Ile
ENST00000437033.6:c.607G>A ENSP00000414254.2:p.Val203Ile
ENST00000476959.5:c.667G>A ENSP00000420269.1:p.Val223Ile
ENST00000482593.5:c.436G>A ENSP00000420613.1:p.Val146Ile
NM_000673.4:c.643G>A NP_000664.2:p.Val215Ile
NM_001166504.1:c.667G>A NP_001159976.1:p.Val223Ile
NM_000673.7:c.607G>A MANE Select NP_000664.3:p.Val203Ile
NM_001166504.2:c.667G>A NP_001159976.1:p.Val223Ile