Canonical Allele Identifier: CA101652564

Gene: ADH1B

Linked Data

• dbSNP Id: rs1048822157
• COSMIC: COSM4465569
• MyVariant Identifiers: chr4:g.100239324G>A (hg19) ; chr4:g.99318167G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318167G>A , CM000666.2:g.99318167G>A	GRCh38
NC_000004.11:g.100239324G>A , CM000666.1:g.100239324G>A	GRCh37
NC_000004.10:g.100458347G>A	NCBI36
NG_011435.1:g.8249C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.138C>T MANE Select	ENSP00000306606.8:p.Ile46=
ENST00000639454.1:c.138C>T	ENSP00000491622.1:p.Ile46=
ENST00000305046.12:c.138C>T	ENSP00000306606.8:p.Ile46=
ENST00000504498.1:n.192C>T
ENST00000506651.5:c.18C>T	ENSP00000425998.2:p.Ile6=
ENST00000515694.4:n.2233C>T
ENST00000625860.2:c.18C>T	ENSP00000486614.1:p.Ile6=
ENST00000632775.1:n.701C>T
NM_000668.5:c.138C>T	NP_000659.2:p.Ile46=
NM_001286650.1:c.18C>T	NP_001273579.1:p.Ile6=
NM_000668.6:c.138C>T MANE Select	NP_000659.2:p.Ile46=
NM_001286650.2:c.18C>T	NP_001273579.1:p.Ile6=