Canonical Allele Identifier: CA2671517295

Gene: ADH1B

Linked Data

• gnomAD v4: 4-99307680-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307680T>C , CM000666.2:g.99307680T>C	GRCh38
NC_000004.11:g.100228837T>C , CM000666.1:g.100228837T>C	GRCh37
NC_000004.10:g.100447860T>C	NCBI36
NG_011435.1:g.18736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.*160A>G MANE Select	ENSP00000306606.8:n.*160A>G
ENST00000305046.12:c.*160A>G	ENSP00000306606.8:n.*160A>G
ENST00000506651.5:c.*160A>G	ENSP00000425998.2:n.*160A>G
ENST00000515694.4:n.3383A>G
ENST00000625860.2:c.*160A>G	ENSP00000486614.1:n.*160A>G
NM_000668.5:c.*160A>G	NP_000659.2:n.*160A>G
NM_001286650.1:c.*160A>G	NP_001273579.1:n.*160A>G
NM_000668.6:c.*160A>G MANE Select	NP_000659.2:n.*160A>G
NM_001286650.2:c.*160A>G	NP_001273579.1:n.*160A>G