Canonical Allele Identifier: CA1480005183
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1721863382
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428428T>A , CM000666.2:g.99428428T>A GRCh38
NC_000004.11:g.100349585T>A , CM000666.1:g.100349585T>A GRCh37
NC_000004.10:g.100568608T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437033.7:c.259+64A>T MANE Select ENSP00000414254.2:n.259+64A>T
ENST00000209665.8:c.295+64A>T ENSP00000209665.4:n.295+64A>T
ENST00000437033.6:c.259+64A>T ENSP00000414254.2:n.259+64A>T
ENST00000474027.1:c.88+64A>T ENSP00000420300.1:n.88+64A>T
ENST00000476959.5:c.319+64A>T ENSP00000420269.1:n.319+64A>T
ENST00000482593.5:c.88+64A>T ENSP00000420613.1:n.88+64A>T
NM_000673.4:c.295+64A>T NP_000664.2:n.295+64A>T
NM_001166504.1:c.319+64A>T NP_001159976.1:n.319+64A>T
NM_000673.7:c.259+64A>T MANE Select NP_000664.3:n.259+64A>T
NM_001166504.2:c.319+64A>T NP_001159976.1:n.319+64A>T
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