Canonical Allele Identifier: CA1595018609

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323375C= , CM000667.2:g.159323375C=	GRCh38
NC_000005.9:g.158750383C= , CM000667.1:g.158750383C=	GRCh37
NC_000005.8:g.158682961C=	NCBI36
NG_009618.1:g.12099G= , LRG_71:g.12099G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2855G=	ENSP00000512849.1:n.-148-2855G=
ENST00000696751.1:c.89-46G=	ENSP00000512850.1:n.89-46G=
ENST00000231228.3:c.89-46G= MANE Select	ENSP00000231228.2:n.89-46G=
ENST00000231228.2:c.89-46G=	ENSP00000231228.2:n.89-46G=
NM_002187.2:c.89-46G= , LRG_71t1:c.89-46G=	NP_002178.2:n.89-46G=
XR_001742945.1:n.148-2159C=
NM_002187.3:c.89-46G= MANE Select	NP_002178.2:n.89-46G=