Canonical Allele Identifier: CA102645377
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs956710811
MyVariant Identifiers: chr4:g.100341375G>C (hg19) chr4:g.99420218G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420218G>C , CM000666.2:g.99420218G>C GRCh38
NC_000004.11:g.100341375G>C , CM000666.1:g.100341375G>C GRCh37
NC_000004.10:g.100560398G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+315C>G MANE Select ENSP00000414254.2:n.825+315C>G
ENST00000209665.8:c.861+315C>G ENSP00000209665.4:n.861+315C>G
ENST00000437033.6:c.825+315C>G ENSP00000414254.2:n.825+315C>G
ENST00000476959.5:c.885+315C>G ENSP00000420269.1:n.885+315C>G
ENST00000482593.5:c.654+315C>G ENSP00000420613.1:n.654+315C>G
NM_000673.4:c.861+315C>G NP_000664.2:n.861+315C>G
NM_001166504.1:c.885+315C>G NP_001159976.1:n.885+315C>G
NM_000673.7:c.825+315C>G MANE Select NP_000664.3:n.825+315C>G
NM_001166504.2:c.885+315C>G NP_001159976.1:n.885+315C>G
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