Canonical Allele Identifier: CA1595017292
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320415_159320418delinsGTCC , CM000667.2:g.159320415_159320418delinsGTCC GRCh38
NC_000005.9:g.158747423_158747426delinsGTCC , CM000667.1:g.158747423_158747426delinsGTCC GRCh37
NC_000005.8:g.158680001_158680004delinsGTCC NCBI36
NG_009618.1:g.15056_15059delinsGGAC , LRG_71:g.15056_15059delinsGGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-46_-43delinsGGAC ENSP00000512849.1:n.-46_-43delinsGGAC
ENST00000696751.1:c.*80_*83delinsGGAC ENSP00000512850.1:n.*80_*83delinsGGAC
ENST00000231228.3:c.585_588delinsGGAC MANE Select ENSP00000231228.2:p.Glu195=
ENST00000231228.2:c.585_588delinsGGAC ENSP00000231228.2:p.Glu195=
NM_002187.2:c.585_588delinsGGAC , LRG_71t1:c.585_588delinsGGAC NP_002178.2:p.Glu195=
NM_002187.3:c.585_588delinsGGAC MANE Select NP_002178.2:p.Glu195=
Search 100 bp 5'
Search 100 bp 3'