Canonical Allele Identifier: CA1479993450
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1579573718
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420240A>G , CM000666.2:g.99420240A>G GRCh38
NC_000004.11:g.100341397A>G , CM000666.1:g.100341397A>G GRCh37
NC_000004.10:g.100560420A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+293T>C MANE Select ENSP00000414254.2:n.825+293T>C
ENST00000209665.8:c.861+293T>C ENSP00000209665.4:n.861+293T>C
ENST00000437033.6:c.825+293T>C ENSP00000414254.2:n.825+293T>C
ENST00000476959.5:c.885+293T>C ENSP00000420269.1:n.885+293T>C
ENST00000482593.5:c.654+293T>C ENSP00000420613.1:n.654+293T>C
NM_000673.4:c.861+293T>C NP_000664.2:n.861+293T>C
NM_001166504.1:c.885+293T>C NP_001159976.1:n.885+293T>C
NM_000673.7:c.825+293T>C MANE Select NP_000664.3:n.825+293T>C
NM_001166504.2:c.885+293T>C NP_001159976.1:n.885+293T>C
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