Canonical Allele Identifier: CA1595018372

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322853T= , CM000667.2:g.159322853T=	GRCh38
NC_000005.9:g.158749861T= , CM000667.1:g.158749861T=	GRCh37
NC_000005.8:g.158682439T=	NCBI36
NG_009618.1:g.12621A= , LRG_71:g.12621A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2333A=	ENSP00000512849.1:n.-148-2333A=
ENST00000696751.1:c.364+201A=	ENSP00000512850.1:n.364+201A=
ENST00000231228.3:c.364+201A= MANE Select	ENSP00000231228.2:n.364+201A=
ENST00000231228.2:c.364+201A=	ENSP00000231228.2:n.364+201A=
NM_002187.2:c.364+201A= , LRG_71t1:c.364+201A=	NP_002178.2:n.364+201A=
XR_001742945.1:n.147+2257T=
NM_002187.3:c.364+201A= MANE Select	NP_002178.2:n.364+201A=