Canonical Allele Identifier: CA1595017428

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320710C= , CM000667.2:g.159320710C=	GRCh38
NC_000005.9:g.158747718C= , CM000667.1:g.158747718C=	GRCh37
NC_000005.8:g.158680296C=	NCBI36
NG_009618.1:g.14764G= , LRG_71:g.14764G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-190G=	ENSP00000512849.1:n.-148-190G=
ENST00000696751.1:c.365-190G=	ENSP00000512850.1:n.365-190G=
ENST00000231228.3:c.483-190G= MANE Select	ENSP00000231228.2:n.483-190G=
ENST00000231228.2:c.483-190G=	ENSP00000231228.2:n.483-190G=
NM_002187.2:c.483-190G= , LRG_71t1:c.483-190G=	NP_002178.2:n.483-190G=
XR_001742945.1:n.147+114C=
NM_002187.3:c.483-190G= MANE Select	NP_002178.2:n.483-190G=