Canonical Allele Identifier: CA2671517349

Gene: ADH1B

Linked Data

• gnomAD v4: 4-99307804-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307804C>A , CM000666.2:g.99307804C>A	GRCh38
NC_000004.11:g.100228961C>A , CM000666.1:g.100228961C>A	GRCh37
NC_000004.10:g.100447984C>A	NCBI36
NG_011435.1:g.18612G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.*36G>T MANE Select	ENSP00000306606.8:n.*36G>T
ENST00000305046.12:c.*36G>T	ENSP00000306606.8:n.*36G>T
ENST00000506651.5:c.*36G>T	ENSP00000425998.2:n.*36G>T
ENST00000515694.4:n.3259G>T
ENST00000625860.2:c.*36G>T	ENSP00000486614.1:n.*36G>T
NM_000668.5:c.*36G>T	NP_000659.2:n.*36G>T
NM_001286650.1:c.*36G>T	NP_001273579.1:n.*36G>T
NM_000668.6:c.*36G>T MANE Select	NP_000659.2:n.*36G>T
NM_001286650.2:c.*36G>T	NP_001273579.1:n.*36G>T