Canonical Allele Identifier: CA1595020699

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328451A= , CM000667.2:g.159328451A=	GRCh38
NC_000005.9:g.158755459A= , CM000667.1:g.158755459A=	GRCh37
NC_000005.8:g.158688037A=	NCBI36
NG_009618.1:g.7023T= , LRG_71:g.7023T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+1981T=	ENSP00000512849.1:n.-149+1981T=
ENST00000696751.1:c.1-1669T=	ENSP00000512850.1:n.1-1669T=
ENST00000696752.1:n.433-1669T=
ENST00000231228.3:c.1-1669T= MANE Select	ENSP00000231228.2:n.1-1669T=
ENST00000231228.2:c.1-1669T=	ENSP00000231228.2:n.1-1669T=
NM_002187.2:c.1-1669T= , LRG_71t1:c.1-1669T=	NP_002178.2:n.1-1669T=
NM_002187.3:c.1-1669T= MANE Select	NP_002178.2:n.1-1669T=