Canonical Allele Identifier: CA102645737

Gene: ADH7

Linked Data

• dbSNP Id: rs199514167
• gnomAD v4: 4-99420529-T-C
• MyVariant Identifiers: chr4:g.100341686T>C (hg19) ; chr4:g.99420529T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420529T>C , CM000666.2:g.99420529T>C	GRCh38
NC_000004.11:g.100341686T>C , CM000666.1:g.100341686T>C	GRCh37
NC_000004.10:g.100560709T>C	NCBI36

Transcript Alleles

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