Canonical Allele Identifier: CA553108837

Gene: ADH7

Linked Data

• dbSNP Id: rs1188412096
• gnomAD v2: 4-100349602-A-G
• gnomAD v4: 4-99428445-A-G
• MyVariant Identifiers: chr4:g.100349602A>G (hg19) ; chr4:g.99428445A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428445A>G , CM000666.2:g.99428445A>G	GRCh38
NC_000004.11:g.100349602A>G , CM000666.1:g.100349602A>G	GRCh37
NC_000004.10:g.100568625A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437033.7:c.259+47T>C MANE Select	ENSP00000414254.2:n.259+47T>C
ENST00000209665.8:c.295+47T>C	ENSP00000209665.4:n.295+47T>C
ENST00000437033.6:c.259+47T>C	ENSP00000414254.2:n.259+47T>C
ENST00000474027.1:c.88+47T>C	ENSP00000420300.1:n.88+47T>C
ENST00000476959.5:c.319+47T>C	ENSP00000420269.1:n.319+47T>C
ENST00000482593.5:c.88+47T>C	ENSP00000420613.1:n.88+47T>C
NM_000673.4:c.295+47T>C	NP_000664.2:n.295+47T>C
NM_001166504.1:c.319+47T>C	NP_001159976.1:n.319+47T>C
NM_000673.7:c.259+47T>C MANE Select	NP_000664.3:n.259+47T>C
NM_001166504.2:c.319+47T>C	NP_001159976.1:n.319+47T>C