Canonical Allele Identifier: CA2676264547
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315934_159315935insAC , CM000667.2:g.159315934_159315935insAC GRCh38
NC_000005.9:g.158742942_158742943insAC , CM000667.1:g.158742942_158742943insAC GRCh37
NC_000005.8:g.158675520_158675521insAC NCBI36
NG_009618.1:g.19539_19540insGT , LRG_71:g.19539_19540insGT

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*166_*167insGT ENSP00000512849.1:n.*166_*167insGT
ENST00000696751.1:c.*648_*649insGT ENSP00000512850.1:n.*648_*649insGT
ENST00000231228.3:c.*166_*167insGT MANE Select ENSP00000231228.2:n.*166_*167insGT
ENST00000231228.2:c.*166_*167insGT ENSP00000231228.2:n.*166_*167insGT
NM_002187.2:c.*166_*167insGT , LRG_71t1:c.*166_*167insGT NP_002178.2:n.*166_*167insGT
NM_002187.3:c.*166_*167insGT MANE Select NP_002178.2:n.*166_*167insGT