Canonical Allele Identifier: CA2695205606

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320343_159320353delinsCCATCTGG , CM000667.2:g.159320343_159320353delinsCCATCTGG	GRCh38
NC_000005.9:g.158747351_158747361delinsCCATCTGG , CM000667.1:g.158747351_158747361delinsCCATCTGG	GRCh37
NC_000005.8:g.158679929_158679939delinsCCATCTGG	NCBI36
NG_009618.1:g.15121_15131delinsCCAGATGG , LRG_71:g.15121_15131delinsCCAGATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.20_30delinsCCAGATGG	ENSP00000512849.1:p.Lys7_Tyr10delinsThrArgTrp
ENST00000696751.1:c.*145_*155delinsCCAGATGG	ENSP00000512850.1:n.*145_*155delinsCCAGATGG
ENST00000231228.3:c.650_660delinsCCAGATGG MANE Select	ENSP00000231228.2:p.Lys217_Tyr220delinsThrArgTrp
ENST00000231228.2:c.650_660delinsCCAGATGG	ENSP00000231228.2:p.Lys217_Tyr220delinsThrArgTrp
NM_002187.2:c.650_660delinsCCAGATGG , LRG_71t1:c.650_660delinsCCAGATGG	NP_002178.2:p.Lys217_Tyr220delinsThrArgTrp
NM_002187.3:c.650_660delinsCCAGATGG MANE Select	NP_002178.2:p.Lys217_Tyr220delinsThrArgTrp