Canonical Allele Identifier: CA362032488
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.14T>C ENSP00000512849.1:p.Val5Ala
ENST00000696751.1:c.*139T>C ENSP00000512850.1:n.*139T>C
ENST00000231228.3:c.644T>C MANE Select ENSP00000231228.2:p.Val215Ala
ENST00000231228.2:c.644T>C ENSP00000231228.2:p.Val215Ala
NM_002187.2:c.644T>C , LRG_71t1:c.644T>C NP_002178.2:p.Val215Ala
NM_002187.3:c.644T>C MANE Select NP_002178.2:p.Val215Ala