Canonical Allele Identifier: CA2769108045

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320012_159320013insTCAAAGTGCAG , CM000667.2:g.159320012_159320013insTCAAAGTGCAG	GRCh38
NC_000005.9:g.158747020_158747021insTCAAAGTGCAG , CM000667.1:g.158747020_158747021insTCAAAGTGCAG	GRCh37
NC_000005.8:g.158679598_158679599insTCAAAGTGCAG	NCBI36
NG_009618.1:g.15461_15462insCTGCACTTTGA , LRG_71:g.15461_15462insCTGCACTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+293_67+294insCTGCACTTTGA	ENSP00000512849.1:n.67+293_67+294insCTGCACTTTGA
ENST00000696751.1:c.*192+293_*192+294insCTGCACTTTGA	ENSP00000512850.1:n.*192+293_*192+294insCTGCACTTTGA
ENST00000231228.3:c.697+293_697+294insCTGCACTTTGA MANE Select	ENSP00000231228.2:n.697+293_697+294insCTGCACTTTGA
ENST00000231228.2:c.697+293_697+294insCTGCACTTTGA	ENSP00000231228.2:n.697+293_697+294insCTGCACTTTGA
NM_002187.2:c.697+293_697+294insCTGCACTTTGA , LRG_71t1:c.697+293_697+294insCTGCACTTTGA	NP_002178.2:n.697+293_697+294insCTGCACTTTGA
NM_002187.3:c.697+293_697+294insCTGCACTTTGA MANE Select	NP_002178.2:n.697+293_697+294insCTGCACTTTGA