Canonical Allele Identifier: CA1595018297

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322641A= , CM000667.2:g.159322641A=	GRCh38
NC_000005.9:g.158749649A= , CM000667.1:g.158749649A=	GRCh37
NC_000005.8:g.158682227A=	NCBI36
NG_009618.1:g.12833T= , LRG_71:g.12833T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2121T=	ENSP00000512849.1:n.-148-2121T=
ENST00000696751.1:c.364+413T=	ENSP00000512850.1:n.364+413T=
ENST00000231228.3:c.365-130T= MANE Select	ENSP00000231228.2:n.365-130T=
ENST00000231228.2:c.365-130T=	ENSP00000231228.2:n.365-130T=
NM_002187.2:c.365-130T= , LRG_71t1:c.365-130T=	NP_002178.2:n.365-130T=
XR_001742945.1:n.147+2045A=
NM_002187.3:c.365-130T= MANE Select	NP_002178.2:n.365-130T=