Canonical Allele Identifier: CA2762794023
Gene: ADH1B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307915C>T , CM000666.2:g.99307915C>T GRCh38
NC_000004.11:g.100229072C>T , CM000666.1:g.100229072C>T GRCh37
NC_000004.10:g.100448095C>T NCBI36
NG_011435.1:g.18501G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.1104-51G>A MANE Select ENSP00000306606.8:n.1104-51G>A
ENST00000639454.1:c.1104-51G>A ENSP00000491622.1:n.1104-51G>A
ENST00000305046.12:c.1104-51G>A ENSP00000306606.8:n.1104-51G>A
ENST00000506651.5:c.984-51G>A ENSP00000425998.2:n.984-51G>A
ENST00000515694.4:n.3199-51G>A
ENST00000625860.2:c.984-51G>A ENSP00000486614.1:n.984-51G>A
NM_000668.5:c.1104-51G>A NP_000659.2:n.1104-51G>A
NM_001286650.1:c.984-51G>A NP_001273579.1:n.984-51G>A
NM_000668.6:c.1104-51G>A MANE Select NP_000659.2:n.1104-51G>A
NM_001286650.2:c.984-51G>A NP_001273579.1:n.984-51G>A
Search 100 bp 5'
Search 100 bp 3'