Canonical Allele Identifier: CA362032489
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320359A>T , CM000667.2:g.159320359A>T GRCh38
NC_000005.9:g.158747367A>T , CM000667.1:g.158747367A>T GRCh37
NC_000005.8:g.158679945A>T NCBI36
NG_009618.1:g.15115T>A , LRG_71:g.15115T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.14T>A ENSP00000512849.1:p.Val5Asp
ENST00000696751.1:c.*139T>A ENSP00000512850.1:n.*139T>A
ENST00000231228.3:c.644T>A MANE Select ENSP00000231228.2:p.Val215Asp
ENST00000231228.2:c.644T>A ENSP00000231228.2:p.Val215Asp
NM_002187.2:c.644T>A , LRG_71t1:c.644T>A NP_002178.2:p.Val215Asp
NM_002187.3:c.644T>A MANE Select NP_002178.2:p.Val215Asp