Canonical Allele Identifier: CA1595017310
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320457C= , CM000667.2:g.159320457C= GRCh38
NC_000005.9:g.158747465C= , CM000667.1:g.158747465C= GRCh37
NC_000005.8:g.158680043C= NCBI36
NG_009618.1:g.15017G= , LRG_71:g.15017G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-85G= ENSP00000512849.1:n.-85G=
ENST00000696751.1:c.*41G= ENSP00000512850.1:n.*41G=
ENST00000231228.3:c.546G= MANE Select ENSP00000231228.2:p.Gly182=
ENST00000231228.2:c.546G= ENSP00000231228.2:p.Gly182=
NM_002187.2:c.546G= , LRG_71t1:c.546G= NP_002178.2:p.Gly182=
XR_001742945.1:n.8C=
NM_002187.3:c.546G= MANE Select NP_002178.2:p.Gly182=