Canonical Allele Identifier: CA1083506174

Gene: IL12B

Linked Data

• dbSNP Id: rs1753985436
• gnomAD v3: 5-159316137-T-TCAAC
• gnomAD v4: 5-159316137-T-TCAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316137_159316138insCAAC , CM000667.2:g.159316137_159316138insCAAC	GRCh38
NC_000005.9:g.158743145_158743146insCAAC , CM000667.1:g.158743145_158743146insCAAC	GRCh37
NC_000005.8:g.158675723_158675724insCAAC	NCBI36
NG_009618.1:g.19336_19337insGTTG , LRG_71:g.19336_19337insGTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1-38_*1-37insGTTG	ENSP00000512849.1:n.*1-38_*1-37insGTTG
ENST00000696751.1:c.*483-38_*483-37insGTTG	ENSP00000512850.1:n.*483-38_*483-37insGTT...
ENST00000231228.3:c.*1-38_*1-37insGTTG MANE Select	ENSP00000231228.2:n.*1-38_*1-37insGTTG
ENST00000231228.2:c.*1-38_*1-37insGTTG	ENSP00000231228.2:n.*1-38_*1-37insGTTG
NM_002187.2:c.*1-38_*1-37insGTTG , LRG_71t1:c.*1-38_*1-37insGTTG	NP_002178.2:n.*1-38_*1-37insGTTG
NM_002187.3:c.*1-38_*1-37insGTTG MANE Select	NP_002178.2:n.*1-38_*1-37insGTTG