Canonical Allele Identifier: CA1595017376
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320599A= , CM000667.2:g.159320599A= GRCh38
NC_000005.9:g.158747607A= , CM000667.1:g.158747607A= GRCh37
NC_000005.8:g.158680185A= NCBI36
NG_009618.1:g.14875T= , LRG_71:g.14875T=

Transcript Alleles

HGVS Amino-acid change
ENST00000231228.3:c.483-79T= MANE Select ENSP00000231228.2:p.=
ENST00000231228.2:c.483-79T= ENSP00000231228.2:p.=
NM_002187.2:c.483-79T= , LRG_71t1:c.483-79T= NP_002178.2:p.=
XR_001742945.1:n.147+3A=
NM_002187.3:c.483-79T= MANE Select NP_002178.2:p.=