Canonical Allele Identifier: CA2671517336
Gene: ADH1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307772dup , CM000666.2:g.99307772dup GRCh38
NC_000004.11:g.100228929dup , CM000666.1:g.100228929dup GRCh37
NC_000004.10:g.100447952dup NCBI36
NG_011435.1:g.18644dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.*68dup MANE Select ENSP00000306606.8:n.*68dup
ENST00000305046.12:c.*68dup ENSP00000306606.8:n.*68dup
ENST00000506651.5:c.*68dup ENSP00000425998.2:n.*68dup
ENST00000515694.4:n.3291dup
ENST00000625860.2:c.*68dup ENSP00000486614.1:n.*68dup
NM_000668.5:c.*68dup NP_000659.2:n.*68dup
NM_001286650.1:c.*68dup NP_001273579.1:n.*68dup
NM_000668.6:c.*68dup MANE Select NP_000659.2:n.*68dup
NM_001286650.2:c.*68dup NP_001273579.1:n.*68dup