Canonical Allele Identifier: CA362033022
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1321430847

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320507G>T , CM000667.2:g.159320507G>T GRCh38
NC_000005.9:g.158747515G>T , CM000667.1:g.158747515G>T GRCh37
NC_000005.8:g.158680093G>T NCBI36
NG_009618.1:g.14967C>A , LRG_71:g.14967C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-135C>A ENSP00000512849.1:n.-135C>A
ENST00000696751.1:c.378C>A ENSP00000512850.1:p.Pro126=
ENST00000231228.3:c.496C>A MANE Select ENSP00000231228.2:p.Gln166Lys
ENST00000231228.2:c.496C>A ENSP00000231228.2:p.Gln166Lys
NM_002187.2:c.496C>A , LRG_71t1:c.496C>A NP_002178.2:p.Gln166Lys
XR_001742945.1:n.58G>T
NM_002187.3:c.496C>A MANE Select NP_002178.2:p.Gln166Lys