Canonical Allele Identifier: CA1595018290

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322632G= , CM000667.2:g.159322632G=	GRCh38
NC_000005.9:g.158749640G= , CM000667.1:g.158749640G=	GRCh37
NC_000005.8:g.158682218G=	NCBI36
NG_009618.1:g.12842C= , LRG_71:g.12842C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2112C=	ENSP00000512849.1:n.-148-2112C=
ENST00000696751.1:c.364+422C=	ENSP00000512850.1:n.364+422C=
ENST00000231228.3:c.365-121C= MANE Select	ENSP00000231228.2:n.365-121C=
ENST00000231228.2:c.365-121C=	ENSP00000231228.2:n.365-121C=
NM_002187.2:c.365-121C= , LRG_71t1:c.365-121C=	NP_002178.2:n.365-121C=
XR_001742945.1:n.147+2036G=
NM_002187.3:c.365-121C= MANE Select	NP_002178.2:n.365-121C=