Canonical Allele Identifier: CA362032168
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320306T>C , CM000667.2:g.159320306T>C GRCh38
NC_000005.9:g.158747314T>C , CM000667.1:g.158747314T>C GRCh37
NC_000005.8:g.158679892T>C NCBI36
NG_009618.1:g.15168A>G , LRG_71:g.15168A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67A>G ENSP00000512849.1:p.Ile23Val
ENST00000696751.1:c.*192A>G ENSP00000512850.1:n.*192A>G
ENST00000231228.3:c.697A>G MANE Select ENSP00000231228.2:p.Ile233Val
ENST00000231228.2:c.697A>G ENSP00000231228.2:p.Ile233Val
NM_002187.2:c.697A>G , LRG_71t1:c.697A>G NP_002178.2:p.Ile233Val
NM_002187.3:c.697A>G MANE Select NP_002178.2:p.Ile233Val