Canonical Allele Identifier: CA1595018643
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323462T= , CM000667.2:g.159323462T= GRCh38
NC_000005.9:g.158750470T= , CM000667.1:g.158750470T= GRCh37
NC_000005.8:g.158683048T= NCBI36
NG_009618.1:g.12012A= , LRG_71:g.12012A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2942A= ENSP00000512849.1:n.-148-2942A=
ENST00000696751.1:c.89-133A= ENSP00000512850.1:n.89-133A=
ENST00000231228.3:c.89-133A= MANE Select ENSP00000231228.2:n.89-133A=
ENST00000231228.2:c.89-133A= ENSP00000231228.2:n.89-133A=
NM_002187.2:c.89-133A= , LRG_71t1:c.89-133A= NP_002178.2:n.89-133A=
XR_001742945.1:n.148-2072T=
NM_002187.3:c.89-133A= MANE Select NP_002178.2:n.89-133A=