Canonical Allele Identifier: CA3020032

Gene: ADH1B

Linked Data

• dbSNP Id: rs746775591
• ExAC: 4:100239177 G / T
• gnomAD v2: 4-100239177-G-T
• gnomAD v4: 4-99318020-G-T
• MyVariant Identifiers: chr4:g.100239177G>T (hg19) ; chr4:g.99318020G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318020G>T , CM000666.2:g.99318020G>T	GRCh38
NC_000004.11:g.100239177G>T , CM000666.1:g.100239177G>T	GRCh37
NC_000004.10:g.100458200G>T	NCBI36
NG_011435.1:g.8396C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.259+26C>A MANE Select	ENSP00000306606.8:n.259+26C>A
ENST00000639454.1:c.259+26C>A	ENSP00000491622.1:n.259+26C>A
ENST00000305046.12:c.259+26C>A	ENSP00000306606.8:n.259+26C>A
ENST00000504498.1:n.339C>A
ENST00000506651.5:c.139+26C>A	ENSP00000425998.2:n.139+26C>A
ENST00000515694.4:n.2354+26C>A
ENST00000625860.2:c.139+26C>A	ENSP00000486614.1:n.139+26C>A
ENST00000632775.1:n.848C>A
NM_000668.5:c.259+26C>A	NP_000659.2:n.259+26C>A
NM_001286650.1:c.139+26C>A	NP_001273579.1:n.139+26C>A
NM_000668.6:c.259+26C>A MANE Select	NP_000659.2:n.259+26C>A
NM_001286650.2:c.139+26C>A	NP_001273579.1:n.139+26C>A