Canonical Allele Identifier: CA1595017089

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159319975T= , CM000667.2:g.159319975T=	GRCh38
NC_000005.9:g.158746983T= , CM000667.1:g.158746983T=	GRCh37
NC_000005.8:g.158679561T=	NCBI36
NG_009618.1:g.15499A= , LRG_71:g.15499A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+331A=	ENSP00000512849.1:n.67+331A=
ENST00000696751.1:c.*192+331A=	ENSP00000512850.1:n.*192+331A=
ENST00000231228.3:c.697+331A= MANE Select	ENSP00000231228.2:n.697+331A=
ENST00000231228.2:c.697+331A=	ENSP00000231228.2:n.697+331A=
NM_002187.2:c.697+331A= , LRG_71t1:c.697+331A=	NP_002178.2:n.697+331A=
NM_002187.3:c.697+331A= MANE Select	NP_002178.2:n.697+331A=