Canonical Allele Identifier: CA800726307

Gene: ADH1B

Linked Data

• dbSNP Id: rs1396015786
• gnomAD v3: 4-99307817-CA-C
• gnomAD v4: 4-99307817-CA-C
• MyVariant Identifiers: chr4:g.100228975del (hg19) ; chr4:g.99307818del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307818del , CM000666.2:g.99307818del	GRCh38
NC_000004.11:g.100228975del , CM000666.1:g.100228975del	GRCh37
NC_000004.10:g.100447998del	NCBI36
NG_011435.1:g.18598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.*22del MANE Select	ENSP00000306606.8:n.*22del
ENST00000305046.12:c.*22del	ENSP00000306606.8:n.*22del
ENST00000506651.5:c.*22del	ENSP00000425998.2:n.*22del
ENST00000515694.4:n.3245del
ENST00000625860.2:c.*22del	ENSP00000486614.1:n.*22del
NM_000668.5:c.*22del	NP_000659.2:n.*22del
NM_001286650.1:c.*22del	NP_001273579.1:n.*22del
NM_000668.6:c.*22del MANE Select	NP_000659.2:n.*22del
NM_001286650.2:c.*22del	NP_001273579.1:n.*22del