Canonical Allele Identifier: CA800706498

Gene: ADH1B

Linked Data

• dbSNP Id: rs1160051766
• MyVariant Identifiers: chr4:g.100242990T>C (hg19) ; chr4:g.99321833T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321833T>C , CM000666.2:g.99321833T>C	GRCh38
NC_000004.11:g.100242990T>C , CM000666.1:g.100242990T>C	GRCh37
NC_000004.10:g.100462013T>C	NCBI36
NG_011435.1:g.4583A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639454.1:c.19-2947A>G	ENSP00000491622.1:n.19-2947A>G