Canonical Allele Identifier: CA1595045194

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159314921T= , CM000667.2:g.159314921T=	GRCh38
NC_000005.9:g.158741929T= , CM000667.1:g.158741929T=	GRCh37
NC_000005.8:g.158674507T=	NCBI36
NG_009618.1:g.20553A= , LRG_71:g.20553A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1180A=	ENSP00000512849.1:n.*1180A=
ENST00000696751.1:c.*1662A=	ENSP00000512850.1:n.*1662A=
ENST00000231228.3:c.*1180A= MANE Select	ENSP00000231228.2:n.*1180A=
ENST00000231228.2:c.*1180A=	ENSP00000231228.2:n.*1180A=
NM_002187.2:c.*1180A= , LRG_71t1:c.*1180A=	NP_002178.2:n.*1180A=
XR_941138.1:n.364-297T=
XR_941138.2:n.431-297T=
NM_002187.3:c.*1180A= MANE Select	NP_002178.2:n.*1180A=