Canonical Allele Identifier: CA1595045691

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315987C= , CM000667.2:g.159315987C=	GRCh38
NC_000005.9:g.158742995C= , CM000667.1:g.158742995C=	GRCh37
NC_000005.8:g.158675573C=	NCBI36
NG_009618.1:g.19487G= , LRG_71:g.19487G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.*114G=	ENSP00000512849.1:n.*114G=
ENST00000696751.1:c.*596G=	ENSP00000512850.1:n.*596G=
ENST00000231228.3:c.*114G= MANE Select	ENSP00000231228.2:n.*114G=
ENST00000231228.2:c.*114G=	ENSP00000231228.2:n.*114G=
NM_002187.2:c.*114G= , LRG_71t1:c.*114G=	NP_002178.2:n.*114G=
NM_002187.3:c.*114G= MANE Select	NP_002178.2:n.*114G=