Canonical Allele Identifier: CA1595045245
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315067_159315069delinsCCT , CM000667.2:g.159315067_159315069delinsCCT GRCh38
NC_000005.9:g.158742075_158742077delinsCCT , CM000667.1:g.158742075_158742077delinsCCT GRCh37
NC_000005.8:g.158674653_158674655delinsCCT NCBI36
NG_009618.1:g.20405_20407delinsAGG , LRG_71:g.20405_20407delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.*1032_*1034delinsAGG ENSP00000512849.1:n.*1032_*1034delinsAGG
ENST00000696751.1:c.*1514_*1516delinsAGG ENSP00000512850.1:n.*1514_*1516delinsAGG
ENST00000231228.3:c.*1032_*1034delinsAGG MANE Select ENSP00000231228.2:n.*1032_*1034delinsAGG
ENST00000231228.2:c.*1032_*1034delinsAGG ENSP00000231228.2:n.*1032_*1034delinsAGG
NM_002187.2:c.*1032_*1034delinsAGG , LRG_71t1:c.*1032_*1034delinsAGG NP_002178.2:n.*1032_*1034delinsAGG
XR_941138.1:n.364-151_364-149delinsCCT
XR_941138.2:n.431-151_431-149delinsCCT
NM_002187.3:c.*1032_*1034delinsAGG MANE Select NP_002178.2:n.*1032_*1034delinsAGG
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