Canonical Allele Identifier: CA1595017331

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320513C= , CM000667.2:g.159320513C=	GRCh38
NC_000005.9:g.158747521C= , CM000667.1:g.158747521C=	GRCh37
NC_000005.8:g.158680099C=	NCBI36
NG_009618.1:g.14961G= , LRG_71:g.14961G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-141G=	ENSP00000512849.1:n.-141G=
ENST00000696751.1:c.372G=	ENSP00000512850.1:p.Leu124=
ENST00000231228.3:c.490G= MANE Select	ENSP00000231228.2:p.Asp164=
ENST00000231228.2:c.490G=	ENSP00000231228.2:p.Asp164=
NM_002187.2:c.490G= , LRG_71t1:c.490G=	NP_002178.2:p.Asp164=
XR_001742945.1:n.64C=
NM_002187.3:c.490G= MANE Select	NP_002178.2:p.Asp164=