Canonical Allele Identifier: CA1595017994

Gene: IL12B

Linked Data

• dbSNP Id: rs1754100936

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321918_159321920del , CM000667.2:g.159321918_159321920del	GRCh38
NC_000005.9:g.158748926_158748928del , CM000667.1:g.158748926_158748928del	GRCh37
NC_000005.8:g.158681504_158681506del	NCBI36
NG_009618.1:g.13557_13559del , LRG_71:g.13557_13559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1397_-148-1395del	ENSP00000512849.1:n.-148-1397_-148-1395del
ENST00000696751.1:c.364+1137_364+1139del	ENSP00000512850.1:n.364+1137_364+1139del
ENST00000231228.3:c.482+477_482+479del MANE Select	ENSP00000231228.2:n.482+477_482+479del
ENST00000231228.2:c.482+477_482+479del	ENSP00000231228.2:n.482+477_482+479del
NM_002187.2:c.482+477_482+479del , LRG_71t1:c.482+477_482+479del	NP_002178.2:n.482+477_482+479del
XR_001742945.1:n.147+1322_147+1324del
NM_002187.3:c.482+477_482+479del MANE Select	NP_002178.2:n.482+477_482+479del