Canonical Allele Identifier: CA1595017996

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321923_159321924delinsGT , CM000667.2:g.159321923_159321924delinsGT	GRCh38
NC_000005.9:g.158748931_158748932delinsGT , CM000667.1:g.158748931_158748932delinsGT	GRCh37
NC_000005.8:g.158681509_158681510delinsGT	NCBI36
NG_009618.1:g.13550_13551delinsAC , LRG_71:g.13550_13551delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1404_-148-1403delinsAC	ENSP00000512849.1:n.-148-1404_-148-1403delinsAC
ENST00000696751.1:c.364+1130_364+1131delinsAC	ENSP00000512850.1:n.364+1130_364+1131delinsAC
ENST00000231228.3:c.482+470_482+471delinsAC MANE Select	ENSP00000231228.2:n.482+470_482+471delinsAC
ENST00000231228.2:c.482+470_482+471delinsAC	ENSP00000231228.2:n.482+470_482+471delinsAC
NM_002187.2:c.482+470_482+471delinsAC , LRG_71t1:c.482+470_482+471delinsAC	NP_002178.2:n.482+470_482+471delinsAC
XR_001742945.1:n.147+1327_147+1328delinsGT
NM_002187.3:c.482+470_482+471delinsAC MANE Select	NP_002178.2:n.482+470_482+471delinsAC