Canonical Allele Identifier: CA1595017336
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320525A= , CM000667.2:g.159320525A= GRCh38
NC_000005.9:g.158747533A= , CM000667.1:g.158747533A= GRCh37
NC_000005.8:g.158680111A= NCBI36
NG_009618.1:g.14949T= , LRG_71:g.14949T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-5T= ENSP00000512849.1:n.-148-5T=
ENST00000696751.1:c.365-5T= ENSP00000512850.1:n.365-5T=
ENST00000231228.3:c.483-5T= MANE Select ENSP00000231228.2:n.483-5T=
ENST00000231228.2:c.483-5T= ENSP00000231228.2:n.483-5T=
NM_002187.2:c.483-5T= , LRG_71t1:c.483-5T= NP_002178.2:n.483-5T=
XR_001742945.1:n.76A=
NM_002187.3:c.483-5T= MANE Select NP_002178.2:n.483-5T=