Canonical Allele Identifier: CA102645497
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs371943586
gnomAD v4: 4-99420423-G-T
MyVariant Identifiers: chr4:g.100341580G>T (hg19) chr4:g.99420423G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420423G>T , CM000666.2:g.99420423G>T GRCh38
NC_000004.11:g.100341580G>T , CM000666.1:g.100341580G>T GRCh37
NC_000004.10:g.100560603G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+110C>A MANE Select ENSP00000414254.2:n.825+110C>A
ENST00000209665.8:c.861+110C>A ENSP00000209665.4:n.861+110C>A
ENST00000437033.6:c.825+110C>A ENSP00000414254.2:n.825+110C>A
ENST00000476959.5:c.885+110C>A ENSP00000420269.1:n.885+110C>A
ENST00000482593.5:c.654+110C>A ENSP00000420613.1:n.654+110C>A
NM_000673.4:c.861+110C>A NP_000664.2:n.861+110C>A
NM_001166504.1:c.885+110C>A NP_001159976.1:n.885+110C>A
NM_000673.7:c.825+110C>A MANE Select NP_000664.3:n.825+110C>A
NM_001166504.2:c.885+110C>A NP_001159976.1:n.885+110C>A
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