Linked Data
ClinVar Variation Id:
962863
ClinVar RCV Id:
RCV001236790
dbSNP Id:
rs1371798524
gnomAD v4:
3-128486359-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128486359G>T , CM000665.2:g.128486359G>T | GRCh38 |
| NC_000003.11:g.128205202G>T , CM000665.1:g.128205202G>T | GRCh37 |
| NC_000003.10:g.129687892G>T | NCBI36 |
| NG_029334.1:g.11829C>A , LRG_295:g.11829C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000487848.6:c.239C>A MANE Plus Clinical | ENSP00000417074.1:p.Thr80Asn | |
| ENST00000696466.1:c.521C>A | ENSP00000512647.1:p.Thr174Asn | |
| ENST00000341105.7:c.239C>A MANE Select | ENSP00000345681.2:p.Thr80Asn | |
| ENST00000341105.6:c.239C>A | ENSP00000345681.2:p.Thr80Asn | |
| ENST00000430265.6:c.239C>A | ENSP00000400259.2:p.Thr80Asn | |
| ENST00000487848.5:c.239C>A | ENSP00000417074.1:p.Thr80Asn | |
| ENST00000492608.1:c.239C>A | ENSP00000418132.1:p.Thr80Asn | |
| NM_001145661.1:c.239C>A , LRG_295t1:c.239C>A | NP_001139133.1:p.Thr80Asn | |
| NM_001145662.1:c.239C>A | NP_001139134.1:p.Thr80Asn | |
| NM_032638.4:c.239C>A , LRG_295t2:c.239C>A | NP_116027.2:p.Thr80Asn | |
| NM_001145661.2:c.239C>A MANE Plus Clinical | NP_001139133.1:p.Thr80Asn | |
| NM_032638.5:c.239C>A MANE Select | NP_116027.2:p.Thr80Asn |