Canonical Allele Identifier: CA2676264543
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315926_159315927insAAAAC , CM000667.2:g.159315926_159315927insAAAAC GRCh38
NC_000005.9:g.158742934_158742935insAAAAC , CM000667.1:g.158742934_158742935insAAAAC GRCh37
NC_000005.8:g.158675512_158675513insAAAAC NCBI36
NG_009618.1:g.19547_19548insGTTTT , LRG_71:g.19547_19548insGTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*174_*175insGTTTT ENSP00000512849.1:n.*174_*175insGTTTT
ENST00000696751.1:c.*656_*657insGTTTT ENSP00000512850.1:n.*656_*657insGTTTT
ENST00000231228.3:c.*174_*175insGTTTT MANE Select ENSP00000231228.2:n.*174_*175insGTTTT
ENST00000231228.2:c.*174_*175insGTTTT ENSP00000231228.2:n.*174_*175insGTTTT
NM_002187.2:c.*174_*175insGTTTT , LRG_71t1:c.*174_*175insGTTTT NP_002178.2:n.*174_*175insGTTTT
NM_002187.3:c.*174_*175insGTTTT MANE Select NP_002178.2:n.*174_*175insGTTTT