Canonical Allele Identifier: CA1595018499

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323131A= , CM000667.2:g.159323131A=	GRCh38
NC_000005.9:g.158750139A= , CM000667.1:g.158750139A=	GRCh37
NC_000005.8:g.158682717A=	NCBI36
NG_009618.1:g.12343T= , LRG_71:g.12343T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-2611T=	ENSP00000512849.1:n.-148-2611T=
ENST00000696751.1:c.287T=	ENSP00000512850.1:p.Val96=
ENST00000231228.3:c.287T= MANE Select	ENSP00000231228.2:p.Val96=
ENST00000231228.2:c.287T=	ENSP00000231228.2:p.Val96=
NM_002187.2:c.287T= , LRG_71t1:c.287T=	NP_002178.2:p.Val96=
XR_001742945.1:n.148-2403A=
NM_002187.3:c.287T= MANE Select	NP_002178.2:p.Val96=