Canonical Allele Identifier: CA1595018420

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322983T= , CM000667.2:g.159322983T=	GRCh38
NC_000005.9:g.158749991T= , CM000667.1:g.158749991T=	GRCh37
NC_000005.8:g.158682569T=	NCBI36
NG_009618.1:g.12491A= , LRG_71:g.12491A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-2463A=	ENSP00000512849.1:n.-148-2463A=
ENST00000696751.1:c.364+71A=	ENSP00000512850.1:n.364+71A=
ENST00000231228.3:c.364+71A= MANE Select	ENSP00000231228.2:n.364+71A=
ENST00000231228.2:c.364+71A=	ENSP00000231228.2:n.364+71A=
NM_002187.2:c.364+71A= , LRG_71t1:c.364+71A=	NP_002178.2:n.364+71A=
XR_001742945.1:n.147+2387T=
NM_002187.3:c.364+71A= MANE Select	NP_002178.2:n.364+71A=