Canonical Allele Identifier: CA1065915989
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1579574394
gnomAD v3: 4-99420907-A-T
gnomAD v4: 4-99420907-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420907A>T , CM000666.2:g.99420907A>T GRCh38
NC_000004.11:g.100342064A>T , CM000666.1:g.100342064A>T GRCh37
NC_000004.10:g.100561087A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-114T>A MANE Select ENSP00000414254.2:n.565-114T>A
ENST00000209665.8:c.601-114T>A ENSP00000209665.4:n.601-114T>A
ENST00000437033.6:c.565-114T>A ENSP00000414254.2:n.565-114T>A
ENST00000476959.5:c.625-114T>A ENSP00000420269.1:n.625-114T>A
ENST00000482593.5:c.394-114T>A ENSP00000420613.1:n.394-114T>A
NM_000673.4:c.601-114T>A NP_000664.2:n.601-114T>A
NM_001166504.1:c.625-114T>A NP_001159976.1:n.625-114T>A
NM_000673.7:c.565-114T>A MANE Select NP_000664.3:n.565-114T>A
NM_001166504.2:c.625-114T>A NP_001159976.1:n.625-114T>A