Canonical Allele Identifier: CA1595020690

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328429_159328430delinsTC , CM000667.2:g.159328429_159328430delinsTC	GRCh38
NC_000005.9:g.158755437_158755438delinsTC , CM000667.1:g.158755437_158755438delinsTC	GRCh37
NC_000005.8:g.158688015_158688016delinsTC	NCBI36
NG_009618.1:g.7044_7045delinsGA , LRG_71:g.7044_7045delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+2002_-149+2003delinsGA	ENSP00000512849.1:n.-149+2002_-149+2003delinsGA
ENST00000696751.1:c.1-1648_1-1647delinsGA	ENSP00000512850.1:n.1-1648_1-1647delinsGA
ENST00000696752.1:n.433-1648_433-1647delinsGA
ENST00000231228.3:c.1-1648_1-1647delinsGA MANE Select	ENSP00000231228.2:n.1-1648_1-1647delinsGA
ENST00000231228.2:c.1-1648_1-1647delinsGA	ENSP00000231228.2:n.1-1648_1-1647delinsGA
NM_002187.2:c.1-1648_1-1647delinsGA , LRG_71t1:c.1-1648_1-1647delinsGA	NP_002178.2:n.1-1648_1-1647delinsGA
NM_002187.3:c.1-1648_1-1647delinsGA MANE Select	NP_002178.2:n.1-1648_1-1647delinsGA