Canonical Allele Identifier: CA1595045242

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315059C= , CM000667.2:g.159315059C=	GRCh38
NC_000005.9:g.158742067C= , CM000667.1:g.158742067C=	GRCh37
NC_000005.8:g.158674645C=	NCBI36
NG_009618.1:g.20415G= , LRG_71:g.20415G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.*1042G=	ENSP00000512849.1:n.*1042G=
ENST00000696751.1:c.*1524G=	ENSP00000512850.1:n.*1524G=
ENST00000231228.3:c.*1042G= MANE Select	ENSP00000231228.2:n.*1042G=
ENST00000231228.2:c.*1042G=	ENSP00000231228.2:n.*1042G=
NM_002187.2:c.*1042G= , LRG_71t1:c.*1042G=	NP_002178.2:n.*1042G=
XR_941138.1:n.364-159C=
XR_941138.2:n.431-159C=
NM_002187.3:c.*1042G= MANE Select	NP_002178.2:n.*1042G=