Canonical Allele Identifier: CA2522261808

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327459_159327460insCTGCGCGGCGTGCGC , CM000667.2:g.159327459_159327460insCTGCGCGGCGTGCGC	GRCh38
NC_000005.9:g.158754467_158754468insCTGCGCGGCGTGCGC , CM000667.1:g.158754467_158754468insCTGCGCGGCGTGCGC	GRCh37
NC_000005.8:g.158687045_158687046insCTGCGCGGCGTGCGC	NCBI36
NG_009618.1:g.8014_8015insGCGCACGCCGCGCAG , LRG_71:g.8014_8015insGCGCACGCCGCGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+2972_-149+2973insGCGCACGCCGCGCAG	ENSP00000512849.1:n.-149+2972_-149+2973insGCGCACGCCGCGCAG
ENST00000696751.1:c.1-678_1-677insGCGCACGCCGCGCAG	ENSP00000512850.1:n.1-678_1-677insGCGCACGCCGCGCAG
ENST00000696752.1:n.433-678_433-677insGCGCACGCCGCGCAG
ENST00000231228.3:c.1-678_1-677insGCGCACGCCGCGCAG MANE Select	ENSP00000231228.2:n.1-678_1-677insGCGCACGCCGCGCAG
ENST00000231228.2:c.1-678_1-677insGCGCACGCCGCGCAG	ENSP00000231228.2:n.1-678_1-677insGCGCACGCCGCGCAG
NM_002187.2:c.1-678_1-677insGCGCACGCCGCGCAG , LRG_71t1:c.1-678_1-677insGCGCACGCCGCGCAG	NP_002178.2:n.1-678_1-677insGCGCACGCCGCGCAG
NM_002187.3:c.1-678_1-677insGCGCACGCCGCGCAG MANE Select	NP_002178.2:n.1-678_1-677insGCGCACGCCGCGCAG