Canonical Allele Identifier: CA1595045244
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315066_159315067delinsTC , CM000667.2:g.159315066_159315067delinsTC GRCh38
NC_000005.9:g.158742074_158742075delinsTC , CM000667.1:g.158742074_158742075delinsTC GRCh37
NC_000005.8:g.158674652_158674653delinsTC NCBI36
NG_009618.1:g.20407_20408delinsGA , LRG_71:g.20407_20408delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1034_*1035delinsGA ENSP00000512849.1:n.*1034_*1035delinsGA
ENST00000696751.1:c.*1516_*1517delinsGA ENSP00000512850.1:n.*1516_*1517delinsGA
ENST00000231228.3:c.*1034_*1035delinsGA MANE Select ENSP00000231228.2:n.*1034_*1035delinsGA
ENST00000231228.2:c.*1034_*1035delinsGA ENSP00000231228.2:n.*1034_*1035delinsGA
NM_002187.2:c.*1034_*1035delinsGA , LRG_71t1:c.*1034_*1035delinsGA NP_002178.2:n.*1034_*1035delinsGA
XR_941138.1:n.364-152_364-151delinsTC
XR_941138.2:n.431-152_431-151delinsTC
NM_002187.3:c.*1034_*1035delinsGA MANE Select NP_002178.2:n.*1034_*1035delinsGA