Linked Data
ClinVar Variation Id:
1510105
ClinVar RCV Id:
RCV002011514
dbSNP Id:
rs2107667768
gnomAD v4:
3-128481107-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128481107A>G , CM000665.2:g.128481107A>G | GRCh38 |
| NC_000003.11:g.128199950A>G , CM000665.1:g.128199950A>G | GRCh37 |
| NC_000003.10:g.129682640A>G | NCBI36 |
| NG_029334.1:g.17081T>C , LRG_295:g.17081T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000487848.6:c.1355T>C MANE Plus Clinical | ENSP00000417074.1:p.Ile452Thr | |
| ENST00000696466.1:c.1637T>C | ENSP00000512647.1:p.Ile546Thr | |
| ENST00000696672.1:c.330T>C | ENSP00000512796.1:p.His110= | |
| ENST00000341105.7:c.1355T>C MANE Select | ENSP00000345681.2:p.Ile452Thr | |
| ENST00000341105.6:c.1355T>C | ENSP00000345681.2:p.Ile452Thr | |
| ENST00000430265.6:c.1313T>C | ENSP00000400259.2:p.Ile438Thr | |
| ENST00000487848.5:c.1355T>C | ENSP00000417074.1:p.Ile452Thr | |
| ENST00000489987.1:n.472T>C | ||
| NM_001145661.1:c.1355T>C , LRG_295t1:c.1355T>C | NP_001139133.1:p.Ile452Thr | |
| NM_001145662.1:c.1313T>C | NP_001139134.1:p.Ile438Thr | |
| NM_032638.4:c.1355T>C , LRG_295t2:c.1355T>C | NP_116027.2:p.Ile452Thr | |
| NM_001145661.2:c.1355T>C MANE Plus Clinical | NP_001139133.1:p.Ile452Thr | |
| NM_032638.5:c.1355T>C MANE Select | NP_116027.2:p.Ile452Thr |