Canonical Allele Identifier: CA362032859
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320441C>T , CM000667.2:g.159320441C>T GRCh38
NC_000005.9:g.158747449C>T , CM000667.1:g.158747449C>T GRCh37
NC_000005.8:g.158680027C>T NCBI36
NG_009618.1:g.15033G>A , LRG_71:g.15033G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-69G>A ENSP00000512849.1:n.-69G>A
ENST00000696751.1:c.*57G>A ENSP00000512850.1:n.*57G>A
ENST00000231228.3:c.562G>A MANE Select ENSP00000231228.2:p.Glu188Lys
ENST00000231228.2:c.562G>A ENSP00000231228.2:p.Glu188Lys
NM_002187.2:c.562G>A , LRG_71t1:c.562G>A NP_002178.2:p.Glu188Lys
NM_002187.3:c.562G>A MANE Select NP_002178.2:p.Glu188Lys