Canonical Allele Identifier: CA1595017190

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320173G= , CM000667.2:g.159320173G=	GRCh38
NC_000005.9:g.158747181G= , CM000667.1:g.158747181G=	GRCh37
NC_000005.8:g.158679759G=	NCBI36
NG_009618.1:g.15301C= , LRG_71:g.15301C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+133C=	ENSP00000512849.1:n.67+133C=
ENST00000696751.1:c.*192+133C=	ENSP00000512850.1:n.*192+133C=
ENST00000231228.3:c.697+133C= MANE Select	ENSP00000231228.2:n.697+133C=
ENST00000231228.2:c.697+133C=	ENSP00000231228.2:n.697+133C=
NM_002187.2:c.697+133C= , LRG_71t1:c.697+133C=	NP_002178.2:n.697+133C=
NM_002187.3:c.697+133C= MANE Select	NP_002178.2:n.697+133C=