Canonical Allele Identifier: CA1595020891

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328941T= , CM000667.2:g.159328941T=	GRCh38
NC_000005.9:g.158755949T= , CM000667.1:g.158755949T=	GRCh37
NC_000005.8:g.158688527T=	NCBI36
NG_009618.1:g.6533A= , LRG_71:g.6533A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1491A=	ENSP00000512849.1:n.-149+1491A=
ENST00000696751.1:c.-1+1491A=	ENSP00000512850.1:n.-1+1491A=
ENST00000696752.1:n.432+1491A=
ENST00000231228.3:c.-1+1491A= MANE Select	ENSP00000231228.2:n.-1+1491A=
ENST00000231228.2:c.-1+1491A=	ENSP00000231228.2:n.-1+1491A=
NM_002187.2:c.-1+1491A= , LRG_71t1:c.-1+1491A=	NP_002178.2:n.-1+1491A=
NM_002187.3:c.-1+1491A= MANE Select	NP_002178.2:n.-1+1491A=