Canonical Allele Identifier: CA102646555

Gene: ADH7

Linked Data

• dbSNP Id: rs939437339
• gnomAD v3: 4-99420894-A-G
• gnomAD v4: 4-99420894-A-G
• MyVariant Identifiers: chr4:g.100342051A>G (hg19) ; chr4:g.99420894A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420894A>G , CM000666.2:g.99420894A>G	GRCh38
NC_000004.11:g.100342051A>G , CM000666.1:g.100342051A>G	GRCh37
NC_000004.10:g.100561074A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.565-101T>C MANE Select	ENSP00000414254.2:n.565-101T>C
ENST00000209665.8:c.601-101T>C	ENSP00000209665.4:n.601-101T>C
ENST00000437033.6:c.565-101T>C	ENSP00000414254.2:n.565-101T>C
ENST00000476959.5:c.625-101T>C	ENSP00000420269.1:n.625-101T>C
ENST00000482593.5:c.394-101T>C	ENSP00000420613.1:n.394-101T>C
NM_000673.4:c.601-101T>C	NP_000664.2:n.601-101T>C
NM_001166504.1:c.625-101T>C	NP_001159976.1:n.625-101T>C
NM_000673.7:c.565-101T>C MANE Select	NP_000664.3:n.565-101T>C
NM_001166504.2:c.625-101T>C	NP_001159976.1:n.625-101T>C