Canonical Allele Identifier: CA1595018339

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322762C= , CM000667.2:g.159322762C=	GRCh38
NC_000005.9:g.158749770C= , CM000667.1:g.158749770C=	GRCh37
NC_000005.8:g.158682348C=	NCBI36
NG_009618.1:g.12712G= , LRG_71:g.12712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2242G=	ENSP00000512849.1:n.-148-2242G=
ENST00000696751.1:c.364+292G=	ENSP00000512850.1:n.364+292G=
ENST00000231228.3:c.365-251G= MANE Select	ENSP00000231228.2:n.365-251G=
ENST00000231228.2:c.365-251G=	ENSP00000231228.2:n.365-251G=
NM_002187.2:c.365-251G= , LRG_71t1:c.365-251G=	NP_002178.2:n.365-251G=
XR_001742945.1:n.147+2166C=
NM_002187.3:c.365-251G= MANE Select	NP_002178.2:n.365-251G=