Canonical Allele Identifier: CA362032976
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320485G>T , CM000667.2:g.159320485G>T GRCh38
NC_000005.9:g.158747493G>T , CM000667.1:g.158747493G>T GRCh37
NC_000005.8:g.158680071G>T NCBI36
NG_009618.1:g.14989C>A , LRG_71:g.14989C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-113C>A ENSP00000512849.1:n.-113C>A
ENST00000696751.1:c.*13C>A ENSP00000512850.1:n.*13C>A
ENST00000231228.3:c.518C>A MANE Select ENSP00000231228.2:p.Ala173Asp
ENST00000231228.2:c.518C>A ENSP00000231228.2:p.Ala173Asp
NM_002187.2:c.518C>A , LRG_71t1:c.518C>A NP_002178.2:p.Ala173Asp
XR_001742945.1:n.36G>T
NM_002187.3:c.518C>A MANE Select NP_002178.2:p.Ala173Asp