Canonical Allele Identifier: CA800703897

Gene: ADH1B

Linked Data

• dbSNP Id: rs1376154299
• gnomAD v3: 4-99317986-T-C
• gnomAD v4: 4-99317986-T-C
• MyVariant Identifiers: chr4:g.100239143T>C (hg19) ; chr4:g.99317986T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99317986T>C , CM000666.2:g.99317986T>C	GRCh38
NC_000004.11:g.100239143T>C , CM000666.1:g.100239143T>C	GRCh37
NC_000004.10:g.100458166T>C	NCBI36
NG_011435.1:g.8430A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.259+60A>G MANE Select	ENSP00000306606.8:n.259+60A>G
ENST00000639454.1:c.259+60A>G	ENSP00000491622.1:n.259+60A>G
ENST00000305046.12:c.259+60A>G	ENSP00000306606.8:n.259+60A>G
ENST00000504498.1:n.373A>G
ENST00000506651.5:c.139+60A>G	ENSP00000425998.2:n.139+60A>G
ENST00000515694.4:n.2354+60A>G
ENST00000625860.2:c.139+60A>G	ENSP00000486614.1:n.139+60A>G
ENST00000632775.1:n.882A>G
NM_000668.5:c.259+60A>G	NP_000659.2:n.259+60A>G
NM_001286650.1:c.139+60A>G	NP_001273579.1:n.139+60A>G
NM_000668.6:c.259+60A>G MANE Select	NP_000659.2:n.259+60A>G
NM_001286650.2:c.139+60A>G	NP_001273579.1:n.139+60A>G