Canonical Allele Identifier: CA362032446
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320350A>C , CM000667.2:g.159320350A>C GRCh38
NC_000005.9:g.158747358A>C , CM000667.1:g.158747358A>C GRCh37
NC_000005.8:g.158679936A>C NCBI36
NG_009618.1:g.15124T>G , LRG_71:g.15124T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.23T>G ENSP00000512849.1:p.Leu8Arg
ENST00000696751.1:c.*148T>G ENSP00000512850.1:n.*148T>G
ENST00000231228.3:c.653T>G MANE Select ENSP00000231228.2:p.Leu218Arg
ENST00000231228.2:c.653T>G ENSP00000231228.2:p.Leu218Arg
NM_002187.2:c.653T>G , LRG_71t1:c.653T>G NP_002178.2:p.Leu218Arg
NM_002187.3:c.653T>G MANE Select NP_002178.2:p.Leu218Arg