Canonical Allele Identifier: CA2676264554
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315944_159315945insGC , CM000667.2:g.159315944_159315945insGC GRCh38
NC_000005.9:g.158742952_158742953insGC , CM000667.1:g.158742952_158742953insGC GRCh37
NC_000005.8:g.158675530_158675531insGC NCBI36
NG_009618.1:g.19529_19530insGC , LRG_71:g.19529_19530insGC

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*156_*157insGC ENSP00000512849.1:n.*156_*157insGC
ENST00000696751.1:c.*638_*639insGC ENSP00000512850.1:n.*638_*639insGC
ENST00000231228.3:c.*156_*157insGC MANE Select ENSP00000231228.2:n.*156_*157insGC
ENST00000231228.2:c.*156_*157insGC ENSP00000231228.2:n.*156_*157insGC
NM_002187.2:c.*156_*157insGC , LRG_71t1:c.*156_*157insGC NP_002178.2:n.*156_*157insGC
NM_002187.3:c.*156_*157insGC MANE Select NP_002178.2:n.*156_*157insGC