Canonical Allele Identifier: CA357479424

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100239291G>C (hg19) ; chr4:g.99318134G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318134G>C , CM000666.2:g.99318134G>C	GRCh38
NC_000004.11:g.100239291G>C , CM000666.1:g.100239291G>C	GRCh37
NC_000004.10:g.100458314G>C	NCBI36
NG_011435.1:g.8282C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.171C>G MANE Select	ENSP00000306606.8:p.Asn57Lys
ENST00000639454.1:c.171C>G	ENSP00000491622.1:p.Asn57Lys
ENST00000305046.12:c.171C>G	ENSP00000306606.8:p.Asn57Lys
ENST00000504498.1:n.225C>G
ENST00000506651.5:c.51C>G	ENSP00000425998.2:p.Asn17Lys
ENST00000515694.4:n.2266C>G
ENST00000625860.2:c.51C>G	ENSP00000486614.1:p.Asn17Lys
ENST00000632775.1:n.734C>G
NM_000668.5:c.171C>G	NP_000659.2:p.Asn57Lys
NM_001286650.1:c.51C>G	NP_001273579.1:p.Asn17Lys
NM_000668.6:c.171C>G MANE Select	NP_000659.2:p.Asn57Lys
NM_001286650.2:c.51C>G	NP_001273579.1:p.Asn17Lys