Canonical Allele Identifier: CA1595017314
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320469C= , CM000667.2:g.159320469C= GRCh38
NC_000005.9:g.158747477C= , CM000667.1:g.158747477C= GRCh37
NC_000005.8:g.158680055C= NCBI36
NG_009618.1:g.15005G= , LRG_71:g.15005G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-97G= ENSP00000512849.1:n.-97G=
ENST00000696751.1:c.*29G= ENSP00000512850.1:n.*29G=
ENST00000231228.3:c.534G= MANE Select ENSP00000231228.2:p.Glu178=
ENST00000231228.2:c.534G= ENSP00000231228.2:p.Glu178=
NM_002187.2:c.534G= , LRG_71t1:c.534G= NP_002178.2:p.Glu178=
XR_001742945.1:n.20C=
NM_002187.3:c.534G= MANE Select NP_002178.2:p.Glu178=