Canonical Allele Identifier: CA362032947
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320470T>G , CM000667.2:g.159320470T>G GRCh38
NC_000005.9:g.158747478T>G , CM000667.1:g.158747478T>G GRCh37
NC_000005.8:g.158680056T>G NCBI36
NG_009618.1:g.15004A>C , LRG_71:g.15004A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-98A>C ENSP00000512849.1:n.-98A>C
ENST00000696751.1:c.*28A>C ENSP00000512850.1:n.*28A>C
ENST00000231228.3:c.533A>C MANE Select ENSP00000231228.2:p.Glu178Ala
ENST00000231228.2:c.533A>C ENSP00000231228.2:p.Glu178Ala
NM_002187.2:c.533A>C , LRG_71t1:c.533A>C NP_002178.2:p.Glu178Ala
XR_001742945.1:n.21T>G
NM_002187.3:c.533A>C MANE Select NP_002178.2:p.Glu178Ala