Linked Data
ClinVar Variation Id:
364855
ClinVar RCV Id:
RCV000368307
dbSNP Id:
rs773285733
gnomAD v4:
9-12702274-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12702274C>G , CM000671.2:g.12702274C>G | GRCh38 |
| NC_000009.11:g.12702274C>G , CM000671.1:g.12702274C>G | GRCh37 |
| NC_000009.10:g.12692274C>G | NCBI36 |
| NG_011705.1:g.13889C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.917C>G (TYRP1) MANE Select | ENSP00000373570.4:p.Thr306Ser | |
| ENST00000381136.2:c.47C>G (TYRP1) | ENSP00000370528.2:p.Thr16Ser | |
| ENST00000381142.3:n.154C>G (TYRP1) | ||
| ENST00000388918.9:c.917C>G (TYRP1) | ENSP00000373570.4:p.Thr306Ser | |
| ENST00000470909.1:n.175C>G (TYRP1) | ||
| NM_000550.2:c.917C>G (TYRP1) | NP_000541.1:p.Thr306Ser | |
| NR_125775.1:n.317-1648G>C (LURAP1L-AS1) | ||
| XR_001746372.2:n.901C>G (TYRP1) | ||
| NM_000550.3:c.917C>G (TYRP1) MANE Select | NP_000541.1:p.Thr306Ser |