Canonical Allele Identifier: CA1595017322

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320496C= , CM000667.2:g.159320496C=	GRCh38
NC_000005.9:g.158747504C= , CM000667.1:g.158747504C=	GRCh37
NC_000005.8:g.158680082C=	NCBI36
NG_009618.1:g.14978G= , LRG_71:g.14978G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-124G=	ENSP00000512849.1:n.-124G=
ENST00000696751.1:c.*2G=	ENSP00000512850.1:n.*2G=
ENST00000231228.3:c.507G= MANE Select	ENSP00000231228.2:p.Thr169=
ENST00000231228.2:c.507G=	ENSP00000231228.2:p.Thr169=
NM_002187.2:c.507G= , LRG_71t1:c.507G=	NP_002178.2:p.Thr169=
XR_001742945.1:n.47C=
NM_002187.3:c.507G= MANE Select	NP_002178.2:p.Thr169=