Canonical Allele Identifier: CA1595017259

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320326C= , CM000667.2:g.159320326C=	GRCh38
NC_000005.9:g.158747334C= , CM000667.1:g.158747334C=	GRCh37
NC_000005.8:g.158679912C=	NCBI36
NG_009618.1:g.15148G= , LRG_71:g.15148G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.47G=	ENSP00000512849.1:p.Ser16=
ENST00000696751.1:c.*172G=	ENSP00000512850.1:n.*172G=
ENST00000231228.3:c.677G= MANE Select	ENSP00000231228.2:p.Ser226=
ENST00000231228.2:c.677G=	ENSP00000231228.2:p.Ser226=
NM_002187.2:c.677G= , LRG_71t1:c.677G=	NP_002178.2:p.Ser226=
NM_002187.3:c.677G= MANE Select	NP_002178.2:p.Ser226=