Canonical Allele Identifier: CA362032741
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1343972120

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320416T>A , CM000667.2:g.159320416T>A GRCh38
NC_000005.9:g.158747424T>A , CM000667.1:g.158747424T>A GRCh37
NC_000005.8:g.158680002T>A NCBI36
NG_009618.1:g.15058A>T , LRG_71:g.15058A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-44A>T ENSP00000512849.1:n.-44A>T
ENST00000696751.1:c.*82A>T ENSP00000512850.1:n.*82A>T
ENST00000231228.3:c.587A>T MANE Select ENSP00000231228.2:p.Asp196Val
ENST00000231228.2:c.587A>T ENSP00000231228.2:p.Asp196Val
NM_002187.2:c.587A>T , LRG_71t1:c.587A>T NP_002178.2:p.Asp196Val
NM_002187.3:c.587A>T MANE Select NP_002178.2:p.Asp196Val