Canonical Allele Identifier: CA362033006
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320500A>T , CM000667.2:g.159320500A>T GRCh38
NC_000005.9:g.158747508A>T , CM000667.1:g.158747508A>T GRCh37
NC_000005.8:g.158680086A>T NCBI36
NG_009618.1:g.14974T>A , LRG_71:g.14974T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-128T>A ENSP00000512849.1:n.-128T>A
ENST00000696751.1:c.385T>A ENSP00000512850.1:p.Ter129Arg
ENST00000231228.3:c.503T>A MANE Select ENSP00000231228.2:p.Val168Glu
ENST00000231228.2:c.503T>A ENSP00000231228.2:p.Val168Glu
NM_002187.2:c.503T>A , LRG_71t1:c.503T>A NP_002178.2:p.Val168Glu
XR_001742945.1:n.51A>T
NM_002187.3:c.503T>A MANE Select NP_002178.2:p.Val168Glu