Canonical Allele Identifier: CA800742432
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1341385814
gnomAD v3: 4-99420798-G-A
gnomAD v4: 4-99420798-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420798G>A , CM000666.2:g.99420798G>A GRCh38
NC_000004.11:g.100341955G>A , CM000666.1:g.100341955G>A GRCh37
NC_000004.10:g.100560978G>A NCBI36

Transcript Alleles

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