Canonical Allele Identifier: CA362032301
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320325G>T , CM000667.2:g.159320325G>T GRCh38
NC_000005.9:g.158747333G>T , CM000667.1:g.158747333G>T GRCh37
NC_000005.8:g.158679911G>T NCBI36
NG_009618.1:g.15149C>A , LRG_71:g.15149C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.48C>A ENSP00000512849.1:p.Ser16Arg
ENST00000696751.1:c.*173C>A ENSP00000512850.1:n.*173C>A
ENST00000231228.3:c.678C>A MANE Select ENSP00000231228.2:p.Ser226Arg
ENST00000231228.2:c.678C>A ENSP00000231228.2:p.Ser226Arg
NM_002187.2:c.678C>A , LRG_71t1:c.678C>A NP_002178.2:p.Ser226Arg
NM_002187.3:c.678C>A MANE Select NP_002178.2:p.Ser226Arg