Canonical Allele Identifier: CA357495886
Gene: ADH1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100229010A>C (hg19) chr4:g.99307853A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307853A>C , CM000666.2:g.99307853A>C GRCh38
NC_000004.11:g.100229010A>C , CM000666.1:g.100229010A>C GRCh37
NC_000004.10:g.100448033A>C NCBI36
NG_011435.1:g.18563T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.1115T>G MANE Select ENSP00000306606.8:p.Val372Gly
ENST00000639454.1:c.1115T>G ENSP00000491622.1:p.Val372Gly
ENST00000305046.12:c.1115T>G ENSP00000306606.8:p.Val372Gly
ENST00000506651.5:c.995T>G ENSP00000425998.2:p.Val332Gly
ENST00000515694.4:n.3210T>G
ENST00000625860.2:c.995T>G ENSP00000486614.1:p.Val332Gly
NM_000668.5:c.1115T>G NP_000659.2:p.Val372Gly
NM_001286650.1:c.995T>G NP_001273579.1:p.Val332Gly
NM_000668.6:c.1115T>G MANE Select NP_000659.2:p.Val372Gly
NM_001286650.2:c.995T>G NP_001273579.1:p.Val332Gly
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