Canonical Allele Identifier: CA1479993598

Gene: ADH7

Linked Data

• dbSNP Id: rs1721618909

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420389A>G , CM000666.2:g.99420389A>G	GRCh38
NC_000004.11:g.100341546A>G , CM000666.1:g.100341546A>G	GRCh37
NC_000004.10:g.100560569A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.825+144T>C MANE Select	ENSP00000414254.2:n.825+144T>C
ENST00000209665.8:c.861+144T>C	ENSP00000209665.4:n.861+144T>C
ENST00000437033.6:c.825+144T>C	ENSP00000414254.2:n.825+144T>C
ENST00000476959.5:c.885+144T>C	ENSP00000420269.1:n.885+144T>C
ENST00000482593.5:c.654+144T>C	ENSP00000420613.1:n.654+144T>C
NM_000673.4:c.861+144T>C	NP_000664.2:n.861+144T>C
NM_001166504.1:c.885+144T>C	NP_001159976.1:n.885+144T>C
NM_000673.7:c.825+144T>C MANE Select	NP_000664.3:n.825+144T>C
NM_001166504.2:c.885+144T>C	NP_001159976.1:n.885+144T>C