Canonical Allele Identifier: CA2695205605

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320340_159320354delinsAATGCAGACGTTATCGA , CM000667.2:g.159320340_159320354delinsAATGCAGACGTTATCGA	GRCh38
NC_000005.9:g.158747348_158747362delinsAATGCAGACGTTATCGA , CM000667.1:g.158747348_158747362delinsAATGCAGACGTTATCGA	GRCh37
NC_000005.8:g.158679926_158679940delinsAATGCAGACGTTATCGA	NCBI36
NG_009618.1:g.15120_15134delinsTCGATAACGTCTGCATT , LRG_71:g.15120_15134delinsTCGATAACGTCTGCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.19_33delinsTCGATAACGTCTGCATT	ENSP00000512849.1:p.Lys7SerfsTer28
ENST00000696751.1:c.*144_*158delinsTCGATAACGTCTGCATT	ENSP00000512850.1:n.*144_*158delinsTCGATAACGTCTGCATT
ENST00000231228.3:c.649_663delinsTCGATAACGTCTGCATT MANE Select	ENSP00000231228.2:p.Lys217SerfsTer28
ENST00000231228.2:c.649_663delinsTCGATAACGTCTGCATT	ENSP00000231228.2:p.Lys217SerfsTer28
NM_002187.2:c.649_663delinsTCGATAACGTCTGCATT , LRG_71t1:c.649_663delinsTCGATAACGTCTGCATT	NP_002178.2:p.Lys217SerfsTer28
NM_002187.3:c.649_663delinsTCGATAACGTCTGCATT MANE Select	NP_002178.2:p.Lys217SerfsTer28