Canonical Allele Identifier: CA564436292
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1191481412

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320469_159320472del , CM000667.2:g.159320469_159320472del GRCh38
NC_000005.9:g.158747477_158747480del , CM000667.1:g.158747477_158747480del GRCh37
NC_000005.8:g.158680055_158680058del NCBI36
NG_009618.1:g.15006_15009del , LRG_71:g.15006_15009del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-96_-93del ENSP00000512849.1:n.-96_-93del
ENST00000696751.1:c.*30_*33del ENSP00000512850.1:n.*30_*33del
ENST00000231228.3:c.535_538del MANE Select ENSP00000231228.2:p.Arg179SerfsTer?
ENST00000231228.2:c.535_538del ENSP00000231228.2:p.Arg179SerfsTer?
NM_002187.2:c.535_538del , LRG_71t1:c.535_538del NP_002178.2:p.Arg179SerfsTer?
XR_001742945.1:n.20_23del
NM_002187.3:c.535_538del MANE Select NP_002178.2:p.Arg179SerfsTer?