Canonical Allele Identifier: CA1595017362
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320576T= , CM000667.2:g.159320576T= GRCh38
NC_000005.9:g.158747584T= , CM000667.1:g.158747584T= GRCh37
NC_000005.8:g.158680162T= NCBI36
NG_009618.1:g.14898A= , LRG_71:g.14898A=

Transcript Alleles

HGVS Amino-acid change
ENST00000231228.3:c.483-56A= MANE Select ENSP00000231228.2:p.=
ENST00000231228.2:c.483-56A= ENSP00000231228.2:p.=
NM_002187.2:c.483-56A= , LRG_71t1:c.483-56A= NP_002178.2:p.=
XR_001742945.1:n.127T=
NM_002187.3:c.483-56A= MANE Select NP_002178.2:p.=