Canonical Allele Identifier: CA362032943
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320468T>A , CM000667.2:g.159320468T>A GRCh38
NC_000005.9:g.158747476T>A , CM000667.1:g.158747476T>A GRCh37
NC_000005.8:g.158680054T>A NCBI36
NG_009618.1:g.15006A>T , LRG_71:g.15006A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-96A>T ENSP00000512849.1:n.-96A>T
ENST00000696751.1:c.*30A>T ENSP00000512850.1:n.*30A>T
ENST00000231228.3:c.535A>T MANE Select ENSP00000231228.2:p.Arg179Ter
ENST00000231228.2:c.535A>T ENSP00000231228.2:p.Arg179Ter
NM_002187.2:c.535A>T , LRG_71t1:c.535A>T NP_002178.2:p.Arg179Ter
XR_001742945.1:n.19T>A
NM_002187.3:c.535A>T MANE Select NP_002178.2:p.Arg179Ter