Canonical Allele Identifier: CA362033011
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320503C>G , CM000667.2:g.159320503C>G GRCh38
NC_000005.9:g.158747511C>G , CM000667.1:g.158747511C>G GRCh37
NC_000005.8:g.158680089C>G NCBI36
NG_009618.1:g.14971G>C , LRG_71:g.14971G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-131G>C ENSP00000512849.1:n.-131G>C
ENST00000696751.1:c.382G>C ENSP00000512850.1:p.Gly128Arg
ENST00000231228.3:c.500G>C MANE Select ENSP00000231228.2:p.Gly167Ala
ENST00000231228.2:c.500G>C ENSP00000231228.2:p.Gly167Ala
NM_002187.2:c.500G>C , LRG_71t1:c.500G>C NP_002178.2:p.Gly167Ala
XR_001742945.1:n.54C>G
NM_002187.3:c.500G>C MANE Select NP_002178.2:p.Gly167Ala