Canonical Allele Identifier: CA357497879
Gene: ADH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100341951C>G (hg19) chr4:g.99420794C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420794C>G , CM000666.2:g.99420794C>G GRCh38
NC_000004.11:g.100341951C>G , CM000666.1:g.100341951C>G GRCh37
NC_000004.10:g.100560974C>G NCBI36

Transcript Alleles

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