Canonical Allele Identifier: CA1595045185

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159314908C= , CM000667.2:g.159314908C=	GRCh38
NC_000005.9:g.158741916C= , CM000667.1:g.158741916C=	GRCh37
NC_000005.8:g.158674494C=	NCBI36
NG_009618.1:g.20566G= , LRG_71:g.20566G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1193G=	ENSP00000512849.1:n.*1193G=
ENST00000696751.1:c.*1675G=	ENSP00000512850.1:n.*1675G=
ENST00000231228.3:c.*1193G= MANE Select	ENSP00000231228.2:n.*1193G=
ENST00000231228.2:c.*1193G=	ENSP00000231228.2:n.*1193G=
NM_002187.2:c.*1193G= , LRG_71t1:c.*1193G=	NP_002178.2:n.*1193G=
XR_941138.1:n.364-310C=
XR_941138.2:n.431-310C=
NM_002187.3:c.*1193G= MANE Select	NP_002178.2:n.*1193G=