Canonical Allele Identifier: CA1595017122

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320049_159320065delinsGCTGTAGTGGAGTGGAT , CM000667.2:g.159320049_159320065delinsGCTGTAGTGGAGTGGAT	GRCh38
NC_000005.9:g.158747057_158747073delinsGCTGTAGTGGAGTGGAT , CM000667.1:g.158747057_158747073delinsGCTGTAGTGGAGTGGAT	GRCh37
NC_000005.8:g.158679635_158679651delinsGCTGTAGTGGAGTGGAT	NCBI36
NG_009618.1:g.15409_15425delinsATCCACTCCACTACAGC , LRG_71:g.15409_15425delinsATCCACTCCACTACAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+241_67+257delinsATCCACTCCACTACAGC	ENSP00000512849.1:n.67+241_67+257delinsATCCACTCCACTACAGC
ENST00000696751.1:c.*192+241_*192+257delinsATCCACTCCACTACAGC	ENSP00000512850.1:n.*192+241_*192+257delinsATCCACTCCACTACAGC
ENST00000231228.3:c.697+241_697+257delinsATCCACTCCACTACAGC MANE Select	ENSP00000231228.2:n.697+241_697+257delinsATCCACTCCACTACAGC
ENST00000231228.2:c.697+241_697+257delinsATCCACTCCACTACAGC	ENSP00000231228.2:n.697+241_697+257delinsATCCACTCCACTACAGC
NM_002187.2:c.697+241_697+257delinsATCCACTCCACTACAGC , LRG_71t1:c.697+241_697+257delinsATCCACTCCACTACAGC	NP_002178.2:n.697+241_697+257delinsATCCACTCCACTACAGC
NM_002187.3:c.697+241_697+257delinsATCCACTCCACTACAGC MANE Select	NP_002178.2:n.697+241_697+257delinsATCCACTCCACTACAGC