Canonical Allele Identifier: CA1595018542

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323217C= , CM000667.2:g.159323217C=	GRCh38
NC_000005.9:g.158750225C= , CM000667.1:g.158750225C=	GRCh37
NC_000005.8:g.158682803C=	NCBI36
NG_009618.1:g.12257G= , LRG_71:g.12257G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2697G=	ENSP00000512849.1:n.-148-2697G=
ENST00000696751.1:c.201G=	ENSP00000512850.1:p.Glu67=
ENST00000231228.3:c.201G= MANE Select	ENSP00000231228.2:p.Glu67=
ENST00000231228.2:c.201G=	ENSP00000231228.2:p.Glu67=
NM_002187.2:c.201G= , LRG_71t1:c.201G=	NP_002178.2:p.Glu67=
XR_001742945.1:n.148-2317C=
NM_002187.3:c.201G= MANE Select	NP_002178.2:p.Glu67=