Canonical Allele Identifier: CA2710492731

Gene: IL12B

Linked Data

• dbSNP Id: rs2113036344

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327136_159327137insC , CM000667.2:g.159327136_159327137insC	GRCh38
NC_000005.9:g.158754144_158754145insC , CM000667.1:g.158754144_158754145insC	GRCh37
NC_000005.8:g.158686722_158686723insC	NCBI36
NG_009618.1:g.8337_8338insG , LRG_71:g.8337_8338insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3295_-149+3296insG	ENSP00000512849.1:n.-149+3295_-149+3296insG
ENST00000696751.1:c.1-355_1-354insG	ENSP00000512850.1:n.1-355_1-354insG
ENST00000696752.1:n.433-355_433-354insG
ENST00000231228.3:c.1-355_1-354insG MANE Select	ENSP00000231228.2:n.1-355_1-354insG
ENST00000231228.2:c.1-355_1-354insG	ENSP00000231228.2:n.1-355_1-354insG
NM_002187.2:c.1-355_1-354insG , LRG_71t1:c.1-355_1-354insG	NP_002178.2:n.1-355_1-354insG
NM_002187.3:c.1-355_1-354insG MANE Select	NP_002178.2:n.1-355_1-354insG