Canonical Allele Identifier: CA800706464
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs1292068684
MyVariant Identifiers: chr4:g.100242943G>C (hg19) chr4:g.99321786G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321786G>C , CM000666.2:g.99321786G>C GRCh38
NC_000004.11:g.100242943G>C , CM000666.1:g.100242943G>C GRCh37
NC_000004.10:g.100461966G>C NCBI36
NG_011435.1:g.4630C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000639454.1:c.19-2900C>G ENSP00000491622.1:n.19-2900C>G
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