Canonical Allele Identifier: CA1595018017

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321990_159321993delinsGGGC , CM000667.2:g.159321990_159321993delinsGGGC	GRCh38
NC_000005.9:g.158748998_158749001delinsGGGC , CM000667.1:g.158748998_158749001delinsGGGC	GRCh37
NC_000005.8:g.158681576_158681579delinsGGGC	NCBI36
NG_009618.1:g.13481_13484delinsGCCC , LRG_71:g.13481_13484delinsGCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-1473_-148-1470delinsGCCC	ENSP00000512849.1:n.-148-1473_-148-1470de...
ENST00000696751.1:c.364+1061_364+1064delinsGCCC	ENSP00000512850.1:n.364+1061_364+1064deli...
ENST00000231228.3:c.482+401_482+404delinsGCCC MANE Select	ENSP00000231228.2:n.482+401_482+404delins...
ENST00000231228.2:c.482+401_482+404delinsGCCC	ENSP00000231228.2:n.482+401_482+404delins...
NM_002187.2:c.482+401_482+404delinsGCCC , LRG_71t1:c.482+401_482+404delinsGCCC	NP_002178.2:n.482+401_482+404delinsGCCC
XR_001742945.1:n.147+1394_147+1397delinsGGGC
NM_002187.3:c.482+401_482+404delinsGCCC MANE Select	NP_002178.2:n.482+401_482+404delinsGCCC