Canonical Allele Identifier: CA1595018085

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322151_159322160delinsCACAGCAGAG , CM000667.2:g.159322151_159322160delinsCACAGCAGAG	GRCh38
NC_000005.9:g.158749159_158749168delinsCACAGCAGAG , CM000667.1:g.158749159_158749168delinsCACAGCAGAG	GRCh37
NC_000005.8:g.158681737_158681746delinsCACAGCAGAG	NCBI36
NG_009618.1:g.13314_13323delinsCTCTGCTGTG , LRG_71:g.13314_13323delinsCTCTGCTGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-1640_-148-1631delinsCTCTGCTGTG	ENSP00000512849.1:n.-148-1640_-148-1631de...
ENST00000696751.1:c.364+894_364+903delinsCTCTGCTGTG	ENSP00000512850.1:n.364+894_364+903delins...
ENST00000231228.3:c.482+234_482+243delinsCTCTGCTGTG MANE Select	ENSP00000231228.2:n.482+234_482+243delins...
ENST00000231228.2:c.482+234_482+243delinsCTCTGCTGTG	ENSP00000231228.2:n.482+234_482+243delins...
NM_002187.2:c.482+234_482+243delinsCTCTGCTGTG , LRG_71t1:c.482+234_482+243delinsCTCTGCTGTG	NP_002178.2:n.482+234_482+243delinsCTCTGC...
XR_001742945.1:n.147+1555_147+1564delinsCACAGCAGAG
NM_002187.3:c.482+234_482+243delinsCTCTGCTGTG MANE Select	NP_002178.2:n.482+234_482+243delinsCTCTGC...