Canonical Allele Identifier: CA440300660

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100239294G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318137G>A , CM000666.2:g.99318137G>A	GRCh38
NC_000004.11:g.100239294G>A , CM000666.1:g.100239294G>A	GRCh37
NC_000004.10:g.100458317G>A	NCBI36
NG_011435.1:g.8279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.168C>T MANE Select	ENSP00000306606.8:p.Gly56=
ENST00000639454.1:c.168C>T	ENSP00000491622.1:p.Gly56=
ENST00000305046.12:c.168C>T	ENSP00000306606.8:p.Gly56=
ENST00000504498.1:n.222C>T
ENST00000506651.5:c.48C>T	ENSP00000425998.2:p.Gly16=
ENST00000515694.4:n.2263C>T
ENST00000625860.2:c.48C>T	ENSP00000486614.1:p.Gly16=
ENST00000632775.1:n.731C>T
NM_000668.5:c.168C>T	NP_000659.2:p.Gly56=
NM_001286650.1:c.48C>T	NP_001273579.1:p.Gly16=
NM_000668.6:c.168C>T MANE Select	NP_000659.2:p.Gly56=
NM_001286650.2:c.48C>T	NP_001273579.1:p.Gly16=