Canonical Allele Identifier: CA1595045199

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159314935T= , CM000667.2:g.159314935T=	GRCh38
NC_000005.9:g.158741943T= , CM000667.1:g.158741943T=	GRCh37
NC_000005.8:g.158674521T=	NCBI36
NG_009618.1:g.20539A= , LRG_71:g.20539A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1166A=	ENSP00000512849.1:n.*1166A=
ENST00000696751.1:c.*1648A=	ENSP00000512850.1:n.*1648A=
ENST00000231228.3:c.*1166A= MANE Select	ENSP00000231228.2:n.*1166A=
ENST00000231228.2:c.*1166A=	ENSP00000231228.2:n.*1166A=
NM_002187.2:c.*1166A= , LRG_71t1:c.*1166A=	NP_002178.2:n.*1166A=
XR_941138.1:n.364-283T=
XR_941138.2:n.431-283T=
NM_002187.3:c.*1166A= MANE Select	NP_002178.2:n.*1166A=