Canonical Allele Identifier: CA800742489
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1203124900
MyVariant Identifiers: chr4:g.100342008A>G (hg19) chr4:g.99420851A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420851A>G , CM000666.2:g.99420851A>G GRCh38
NC_000004.11:g.100342008A>G , CM000666.1:g.100342008A>G GRCh37
NC_000004.10:g.100561031A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-58T>C MANE Select ENSP00000414254.2:n.565-58T>C
ENST00000209665.8:c.601-58T>C ENSP00000209665.4:n.601-58T>C
ENST00000437033.6:c.565-58T>C ENSP00000414254.2:n.565-58T>C
ENST00000476959.5:c.625-58T>C ENSP00000420269.1:n.625-58T>C
ENST00000482593.5:c.394-58T>C ENSP00000420613.1:n.394-58T>C
NM_000673.4:c.601-58T>C NP_000664.2:n.601-58T>C
NM_001166504.1:c.625-58T>C NP_001159976.1:n.625-58T>C
NM_000673.7:c.565-58T>C MANE Select NP_000664.3:n.565-58T>C
NM_001166504.2:c.625-58T>C NP_001159976.1:n.625-58T>C
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