Canonical Allele Identifier: CA2676264541
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315925_159315926insCC , CM000667.2:g.159315925_159315926insCC GRCh38
NC_000005.9:g.158742933_158742934insCC , CM000667.1:g.158742933_158742934insCC GRCh37
NC_000005.8:g.158675511_158675512insCC NCBI36
NG_009618.1:g.19548_19549insGG , LRG_71:g.19548_19549insGG

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*175_*176insGG ENSP00000512849.1:n.*175_*176insGG
ENST00000696751.1:c.*657_*658insGG ENSP00000512850.1:n.*657_*658insGG
ENST00000231228.3:c.*175_*176insGG MANE Select ENSP00000231228.2:n.*175_*176insGG
ENST00000231228.2:c.*175_*176insGG ENSP00000231228.2:n.*175_*176insGG
NM_002187.2:c.*175_*176insGG , LRG_71t1:c.*175_*176insGG NP_002178.2:n.*175_*176insGG
NM_002187.3:c.*175_*176insGG MANE Select NP_002178.2:n.*175_*176insGG