Canonical Allele Identifier: CA1595018493

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323119G= , CM000667.2:g.159323119G=	GRCh38
NC_000005.9:g.158750127G= , CM000667.1:g.158750127G=	GRCh37
NC_000005.8:g.158682705G=	NCBI36
NG_009618.1:g.12355C= , LRG_71:g.12355C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2599C=	ENSP00000512849.1:n.-148-2599C=
ENST00000696751.1:c.299C=	ENSP00000512850.1:p.Ser100=
ENST00000231228.3:c.299C= MANE Select	ENSP00000231228.2:p.Ser100=
ENST00000231228.2:c.299C=	ENSP00000231228.2:p.Ser100=
NM_002187.2:c.299C= , LRG_71t1:c.299C=	NP_002178.2:p.Ser100=
XR_001742945.1:n.148-2415G=
NM_002187.3:c.299C= MANE Select	NP_002178.2:p.Ser100=