Canonical Allele Identifier: CA362032926
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320460T>G , CM000667.2:g.159320460T>G GRCh38
NC_000005.9:g.158747468T>G , CM000667.1:g.158747468T>G GRCh37
NC_000005.8:g.158680046T>G NCBI36
NG_009618.1:g.15014A>C , LRG_71:g.15014A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-88A>C ENSP00000512849.1:n.-88A>C
ENST00000696751.1:c.*38A>C ENSP00000512850.1:n.*38A>C
ENST00000231228.3:c.543A>C MANE Select ENSP00000231228.2:p.Arg181Ser
ENST00000231228.2:c.543A>C ENSP00000231228.2:p.Arg181Ser
NM_002187.2:c.543A>C , LRG_71t1:c.543A>C NP_002178.2:p.Arg181Ser
XR_001742945.1:n.11T>G
NM_002187.3:c.543A>C MANE Select NP_002178.2:p.Arg181Ser