Canonical Allele Identifier: CA362033004
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320500A>C , CM000667.2:g.159320500A>C GRCh38
NC_000005.9:g.158747508A>C , CM000667.1:g.158747508A>C GRCh37
NC_000005.8:g.158680086A>C NCBI36
NG_009618.1:g.14974T>G , LRG_71:g.14974T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-128T>G ENSP00000512849.1:n.-128T>G
ENST00000696751.1:c.385T>G ENSP00000512850.1:p.Ter129Gly
ENST00000231228.3:c.503T>G MANE Select ENSP00000231228.2:p.Val168Gly
ENST00000231228.2:c.503T>G ENSP00000231228.2:p.Val168Gly
NM_002187.2:c.503T>G , LRG_71t1:c.503T>G NP_002178.2:p.Val168Gly
XR_001742945.1:n.51A>C
NM_002187.3:c.503T>G MANE Select NP_002178.2:p.Val168Gly