Canonical Allele Identifier: CA362032930
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320462T>A , CM000667.2:g.159320462T>A GRCh38
NC_000005.9:g.158747470T>A , CM000667.1:g.158747470T>A GRCh37
NC_000005.8:g.158680048T>A NCBI36
NG_009618.1:g.15012A>T , LRG_71:g.15012A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-90A>T ENSP00000512849.1:n.-90A>T
ENST00000696751.1:c.*36A>T ENSP00000512850.1:n.*36A>T
ENST00000231228.3:c.541A>T MANE Select ENSP00000231228.2:p.Arg181Ter
ENST00000231228.2:c.541A>T ENSP00000231228.2:p.Arg181Ter
NM_002187.2:c.541A>T , LRG_71t1:c.541A>T NP_002178.2:p.Arg181Ter
XR_001742945.1:n.13T>A
NM_002187.3:c.541A>T MANE Select NP_002178.2:p.Arg181Ter