Canonical Allele Identifier: CA800742519

Gene: ADH7

Linked Data

• dbSNP Id: rs1162514903
• gnomAD v4: 4-99420891-C-T
• MyVariant Identifiers: chr4:g.100342048C>T (hg19) ; chr4:g.99420891C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420891C>T , CM000666.2:g.99420891C>T	GRCh38
NC_000004.11:g.100342048C>T , CM000666.1:g.100342048C>T	GRCh37
NC_000004.10:g.100561071C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.565-98G>A MANE Select	ENSP00000414254.2:n.565-98G>A
ENST00000209665.8:c.601-98G>A	ENSP00000209665.4:n.601-98G>A
ENST00000437033.6:c.565-98G>A	ENSP00000414254.2:n.565-98G>A
ENST00000476959.5:c.625-98G>A	ENSP00000420269.1:n.625-98G>A
ENST00000482593.5:c.394-98G>A	ENSP00000420613.1:n.394-98G>A
NM_000673.4:c.601-98G>A	NP_000664.2:n.601-98G>A
NM_001166504.1:c.625-98G>A	NP_001159976.1:n.625-98G>A
NM_000673.7:c.565-98G>A MANE Select	NP_000664.3:n.565-98G>A
NM_001166504.2:c.625-98G>A	NP_001159976.1:n.625-98G>A