Linked Data
ClinVar Variation Id:
223215
ClinVar RCV Id:
RCV000208823
dbSNP Id:
rs869025655
COSMIC:
COSM14389
CIViC:
CA357068
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10146625T>G , CM000665.2:g.10146625T>G | GRCh38 |
| NC_000003.11:g.10188309T>G , CM000665.1:g.10188309T>G | GRCh37 |
| NC_000003.10:g.10163309T>G | NCBI36 |
| NG_008212.3:g.9991T>G , LRG_322:g.9991T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*129T>G | ENSP00000512434.1:n.*129T>G | |
| ENST00000696143.1:c.600-3162T>G | ENSP00000512435.1:n.600-3162T>G | |
| ENST00000696153.1:c.452T>G | ENSP00000512444.1:p.Ile151Ser | |
| ENST00000256474.3:c.452T>G MANE Select | ENSP00000256474.3:p.Ile151Ser | |
| ENST00000256474.2:c.452T>G | ENSP00000256474.2:p.Ile151Ser | |
| ENST00000345392.2:c.341-3162T>G | ENSP00000344757.2:n.341-3162T>G | |
| ENST00000477538.1:n.588T>G | ||
| NM_000551.3:c.452T>G , LRG_322t1:c.452T>G | NP_000542.1:p.Ile151Ser | |
| NM_198156.2:c.341-3162T>G | NP_937799.1:n.341-3162T>G | |
| NM_001354723.1:c.*18-3162T>G | NP_001341652.1:n.*18-3162T>G | |
| NM_000551.4:c.452T>G MANE Select | NP_000542.1:p.Ile151Ser | |
| NM_001354723.2:c.*18-3162T>G | NP_001341652.1:n.*18-3162T>G | |
| NM_198156.3:c.341-3162T>G | NP_937799.1:n.341-3162T>G |