Canonical Allele Identifier: CA357479198

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100239247C>A (hg19) ; chr4:g.99318090C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318090C>A , CM000666.2:g.99318090C>A	GRCh38
NC_000004.11:g.100239247C>A , CM000666.1:g.100239247C>A	GRCh37
NC_000004.10:g.100458270C>A	NCBI36
NG_011435.1:g.8326G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.215G>T MANE Select	ENSP00000306606.8:p.Gly72Val
ENST00000639454.1:c.215G>T	ENSP00000491622.1:p.Gly72Val
ENST00000305046.12:c.215G>T	ENSP00000306606.8:p.Gly72Val
ENST00000504498.1:n.269G>T
ENST00000506651.5:c.95G>T	ENSP00000425998.2:p.Gly32Val
ENST00000515694.4:n.2310G>T
ENST00000625860.2:c.95G>T	ENSP00000486614.1:p.Gly32Val
ENST00000632775.1:n.778G>T
NM_000668.5:c.215G>T	NP_000659.2:p.Gly72Val
NM_001286650.1:c.95G>T	NP_001273579.1:p.Gly32Val
NM_000668.6:c.215G>T MANE Select	NP_000659.2:p.Gly72Val
NM_001286650.2:c.95G>T	NP_001273579.1:p.Gly32Val