Canonical Allele Identifier: CA800741669
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1371654138
MyVariant Identifiers: chr4:g.100341414C>T (hg19) chr4:g.99420257C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420257C>T , CM000666.2:g.99420257C>T GRCh38
NC_000004.11:g.100341414C>T , CM000666.1:g.100341414C>T GRCh37
NC_000004.10:g.100560437C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+276G>A MANE Select ENSP00000414254.2:n.825+276G>A
ENST00000209665.8:c.861+276G>A ENSP00000209665.4:n.861+276G>A
ENST00000437033.6:c.825+276G>A ENSP00000414254.2:n.825+276G>A
ENST00000476959.5:c.885+276G>A ENSP00000420269.1:n.885+276G>A
ENST00000482593.5:c.654+276G>A ENSP00000420613.1:n.654+276G>A
NM_000673.4:c.861+276G>A NP_000664.2:n.861+276G>A
NM_001166504.1:c.885+276G>A NP_001159976.1:n.885+276G>A
NM_000673.7:c.825+276G>A MANE Select NP_000664.3:n.825+276G>A
NM_001166504.2:c.885+276G>A NP_001159976.1:n.885+276G>A
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