Canonical Allele Identifier: CA1595020250

Gene: IL12B

Linked Data

• dbSNP Id: rs1754209536

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327409_159327410del , CM000667.2:g.159327409_159327410del	GRCh38
NC_000005.9:g.158754417_158754418del , CM000667.1:g.158754417_158754418del	GRCh37
NC_000005.8:g.158686995_158686996del	NCBI36
NG_009618.1:g.8065_8066del , LRG_71:g.8065_8066del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3023_-149+3024del	ENSP00000512849.1:n.-149+3023_-149+3024del
ENST00000696751.1:c.1-627_1-626del	ENSP00000512850.1:n.1-627_1-626del
ENST00000696752.1:n.433-627_433-626del
ENST00000231228.3:c.1-627_1-626del MANE Select	ENSP00000231228.2:n.1-627_1-626del
ENST00000231228.2:c.1-627_1-626del	ENSP00000231228.2:n.1-627_1-626del
NM_002187.2:c.1-627_1-626del , LRG_71t1:c.1-627_1-626del	NP_002178.2:n.1-627_1-626del
NM_002187.3:c.1-627_1-626del MANE Select	NP_002178.2:n.1-627_1-626del