Linked Data
ClinVar Variation Id:
766745
ClinVar RCV Id:
RCV001438641
dbSNP Id:
rs1462031219
gnomAD v2:
3-128205069-C-T
gnomAD v4:
3-128486226-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128486226C>T , CM000665.2:g.128486226C>T | GRCh38 |
| NC_000003.11:g.128205069C>T , CM000665.1:g.128205069C>T | GRCh37 |
| NC_000003.10:g.129687759C>T | NCBI36 |
| NG_029334.1:g.11962G>A , LRG_295:g.11962G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000487848.6:c.372G>A MANE Plus Clinical | ENSP00000417074.1:p.Thr124= | |
| ENST00000696466.1:c.654G>A | ENSP00000512647.1:p.Thr218= | |
| ENST00000341105.7:c.372G>A MANE Select | ENSP00000345681.2:p.Thr124= | |
| ENST00000341105.6:c.372G>A | ENSP00000345681.2:p.Thr124= | |
| ENST00000430265.6:c.372G>A | ENSP00000400259.2:p.Thr124= | |
| ENST00000487848.5:c.372G>A | ENSP00000417074.1:p.Thr124= | |
| ENST00000492608.1:c.372G>A | ENSP00000418132.1:p.Thr124= | |
| NM_001145661.1:c.372G>A , LRG_295t1:c.372G>A | NP_001139133.1:p.Thr124= | |
| NM_001145662.1:c.372G>A | NP_001139134.1:p.Thr124= | |
| NM_032638.4:c.372G>A , LRG_295t2:c.372G>A | NP_116027.2:p.Thr124= | |
| NM_001145661.2:c.372G>A MANE Plus Clinical | NP_001139133.1:p.Thr124= | |
| NM_032638.5:c.372G>A MANE Select | NP_116027.2:p.Thr124= |