Canonical Allele Identifier: CA1595020174

Gene: IL12B

Linked Data

• dbSNP Id: rs1754206190

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327212_159327213del , CM000667.2:g.159327212_159327213del	GRCh38
NC_000005.9:g.158754220_158754221del , CM000667.1:g.158754220_158754221del	GRCh37
NC_000005.8:g.158686798_158686799del	NCBI36
NG_009618.1:g.8267_8268del , LRG_71:g.8267_8268del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+3225_-149+3226del	ENSP00000512849.1:n.-149+3225_-149+3226de...
ENST00000696751.1:c.1-425_1-424del	ENSP00000512850.1:n.1-425_1-424del
ENST00000696752.1:n.433-425_433-424del
ENST00000231228.3:c.1-425_1-424del MANE Select	ENSP00000231228.2:n.1-425_1-424del
ENST00000231228.2:c.1-425_1-424del	ENSP00000231228.2:n.1-425_1-424del
NM_002187.2:c.1-425_1-424del , LRG_71t1:c.1-425_1-424del	NP_002178.2:n.1-425_1-424del
NM_002187.3:c.1-425_1-424del MANE Select	NP_002178.2:n.1-425_1-424del