Canonical Allele Identifier: CA3538673
Gene: IL12B HGNC NCBI

Linked Data

ClinVar Variation Id: 352572
ClinVar RCV Id: RCV000531175
dbSNP Id: rs3213119

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316780C>A , CM000667.2:g.159316780C>A GRCh38
NC_000005.9:g.158743788C>A , CM000667.1:g.158743788C>A GRCh37
NC_000005.8:g.158676366C>A NCBI36
NG_009618.1:g.18694G>T , LRG_71:g.18694G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.262G>T ENSP00000512849.1:p.Val88Phe
ENST00000696751.1:c.*387G>T ENSP00000512850.1:n.*387G>T
ENST00000231228.3:c.892G>T MANE Select ENSP00000231228.2:p.Val298Phe
ENST00000231228.2:c.892G>T ENSP00000231228.2:p.Val298Phe
NM_002187.2:c.892G>T , LRG_71t1:c.892G>T NP_002178.2:p.Val298Phe
NM_002187.3:c.892G>T MANE Select NP_002178.2:p.Val298Phe