Canonical Allele Identifier: CA1595020235

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327383T= , CM000667.2:g.159327383T=	GRCh38
NC_000005.9:g.158754391T= , CM000667.1:g.158754391T=	GRCh37
NC_000005.8:g.158686969T=	NCBI36
NG_009618.1:g.8091A= , LRG_71:g.8091A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3049A=	ENSP00000512849.1:n.-149+3049A=
ENST00000696751.1:c.1-601A=	ENSP00000512850.1:n.1-601A=
ENST00000696752.1:n.433-601A=
ENST00000231228.3:c.1-601A= MANE Select	ENSP00000231228.2:n.1-601A=
ENST00000231228.2:c.1-601A=	ENSP00000231228.2:n.1-601A=
NM_002187.2:c.1-601A= , LRG_71t1:c.1-601A=	NP_002178.2:n.1-601A=
NM_002187.3:c.1-601A= MANE Select	NP_002178.2:n.1-601A=