Canonical Allele Identifier: CA357497663
Gene: ADH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100341839T>G (hg19) chr4:g.99420682T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420682T>G , CM000666.2:g.99420682T>G GRCh38
NC_000004.11:g.100341839T>G , CM000666.1:g.100341839T>G GRCh37
NC_000004.10:g.100560862T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.676A>C MANE Select ENSP00000414254.2:p.Lys226Gln
ENST00000209665.8:c.712A>C ENSP00000209665.4:p.Lys238Gln
ENST00000437033.6:c.676A>C ENSP00000414254.2:p.Lys226Gln
ENST00000476959.5:c.736A>C ENSP00000420269.1:p.Lys246Gln
ENST00000482593.5:c.505A>C ENSP00000420613.1:p.Lys169Gln
NM_000673.4:c.712A>C NP_000664.2:p.Lys238Gln
NM_001166504.1:c.736A>C NP_001159976.1:p.Lys246Gln
NM_000673.7:c.676A>C MANE Select NP_000664.3:p.Lys226Gln
NM_001166504.2:c.736A>C NP_001159976.1:p.Lys246Gln
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