Canonical Allele Identifier: CA1595017317

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320481T= , CM000667.2:g.159320481T=	GRCh38
NC_000005.9:g.158747489T= , CM000667.1:g.158747489T=	GRCh37
NC_000005.8:g.158680067T=	NCBI36
NG_009618.1:g.14993A= , LRG_71:g.14993A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-109A=	ENSP00000512849.1:n.-109A=
ENST00000696751.1:c.*17A=	ENSP00000512850.1:n.*17A=
ENST00000231228.3:c.522A= MANE Select	ENSP00000231228.2:p.Thr174=
ENST00000231228.2:c.522A=	ENSP00000231228.2:p.Thr174=
NM_002187.2:c.522A= , LRG_71t1:c.522A=	NP_002178.2:p.Thr174=
XR_001742945.1:n.32T=
NM_002187.3:c.522A= MANE Select	NP_002178.2:p.Thr174=