Canonical Allele Identifier: CA3020065
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs752859831
gnomAD v4: 4-99318175-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318175C>T , CM000666.2:g.99318175C>T GRCh38
NC_000004.11:g.100239332C>T , CM000666.1:g.100239332C>T GRCh37
NC_000004.10:g.100458355C>T NCBI36
NG_011435.1:g.8241G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.130G>A MANE Select ENSP00000306606.8:p.Val44Ile
ENST00000639454.1:c.130G>A ENSP00000491622.1:p.Val44Ile
ENST00000305046.12:c.130G>A ENSP00000306606.8:p.Val44Ile
ENST00000504498.1:n.184G>A
ENST00000506651.5:c.10G>A ENSP00000425998.2:p.Val4Ile
ENST00000515694.4:n.2225G>A
ENST00000625860.2:c.10G>A ENSP00000486614.1:p.Val4Ile
ENST00000632775.1:n.693G>A
NM_000668.5:c.130G>A NP_000659.2:p.Val44Ile
NM_001286650.1:c.10G>A NP_001273579.1:p.Val4Ile
NM_000668.6:c.130G>A MANE Select NP_000659.2:p.Val44Ile
NM_001286650.2:c.10G>A NP_001273579.1:p.Val4Ile