Canonical Allele Identifier: CA2769108355
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315028C>G , CM000667.2:g.159315028C>G GRCh38
NC_000005.9:g.158742036C>G , CM000667.1:g.158742036C>G GRCh37
NC_000005.8:g.158674614C>G NCBI36
NG_009618.1:g.20446G>C , LRG_71:g.20446G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.*1073G>C ENSP00000512849.1:n.*1073G>C
ENST00000696751.1:c.*1555G>C ENSP00000512850.1:n.*1555G>C
ENST00000231228.3:c.*1073G>C MANE Select ENSP00000231228.2:n.*1073G>C
ENST00000231228.2:c.*1073G>C ENSP00000231228.2:n.*1073G>C
NM_002187.2:c.*1073G>C , LRG_71t1:c.*1073G>C NP_002178.2:n.*1073G>C
XR_941138.1:n.364-190C>G
XR_941138.2:n.431-190C>G
NM_002187.3:c.*1073G>C MANE Select NP_002178.2:n.*1073G>C
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