Canonical Allele Identifier: CA1595018094

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322180A= , CM000667.2:g.159322180A=	GRCh38
NC_000005.9:g.158749188A= , CM000667.1:g.158749188A=	GRCh37
NC_000005.8:g.158681766A=	NCBI36
NG_009618.1:g.13294T= , LRG_71:g.13294T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1660T=	ENSP00000512849.1:n.-148-1660T=
ENST00000696751.1:c.364+874T=	ENSP00000512850.1:n.364+874T=
ENST00000231228.3:c.482+214T= MANE Select	ENSP00000231228.2:n.482+214T=
ENST00000231228.2:c.482+214T=	ENSP00000231228.2:n.482+214T=
NM_002187.2:c.482+214T= , LRG_71t1:c.482+214T=	NP_002178.2:n.482+214T=
XR_001742945.1:n.147+1584A=
NM_002187.3:c.482+214T= MANE Select	NP_002178.2:n.482+214T=