Canonical Allele Identifier: CA1595017977

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321883_159321884delinsTG , CM000667.2:g.159321883_159321884delinsTG	GRCh38
NC_000005.9:g.158748891_158748892delinsTG , CM000667.1:g.158748891_158748892delinsTG	GRCh37
NC_000005.8:g.158681469_158681470delinsTG	NCBI36
NG_009618.1:g.13590_13591delinsCA , LRG_71:g.13590_13591delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1364_-148-1363delinsCA	ENSP00000512849.1:n.-148-1364_-148-1363delinsCA
ENST00000696751.1:c.364+1170_364+1171delinsCA	ENSP00000512850.1:n.364+1170_364+1171delinsCA
ENST00000231228.3:c.482+510_482+511delinsCA MANE Select	ENSP00000231228.2:n.482+510_482+511delinsCA
ENST00000231228.2:c.482+510_482+511delinsCA	ENSP00000231228.2:n.482+510_482+511delinsCA
NM_002187.2:c.482+510_482+511delinsCA , LRG_71t1:c.482+510_482+511delinsCA	NP_002178.2:n.482+510_482+511delinsCA
XR_001742945.1:n.147+1287_147+1288delinsTG
NM_002187.3:c.482+510_482+511delinsCA MANE Select	NP_002178.2:n.482+510_482+511delinsCA