Linked Data
MyVariant Identifiers:
chr9:g.12702377T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12702377T>C , CM000671.2:g.12702377T>C | GRCh38 |
| NC_000009.11:g.12702377T>C , CM000671.1:g.12702377T>C | GRCh37 |
| NC_000009.10:g.12692377T>C | NCBI36 |
| NG_011705.1:g.13992T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.1020T>C (TYRP1) MANE Select | ENSP00000373570.4:p.Gly340= | |
| ENST00000381136.2:c.150T>C (TYRP1) | ENSP00000370528.2:p.Gly50= | |
| ENST00000381142.3:n.257T>C (TYRP1) | ||
| ENST00000388918.9:c.1020T>C (TYRP1) | ENSP00000373570.4:p.Gly340= | |
| ENST00000470909.1:n.278T>C (TYRP1) | ||
| NM_000550.2:c.1020T>C (TYRP1) | NP_000541.1:p.Gly340= | |
| NR_125775.1:n.317-1751A>G (LURAP1L-AS1) | ||
| XR_001746372.2:n.1004T>C (TYRP1) | ||
| NM_000550.3:c.1020T>C (TYRP1) MANE Select | NP_000541.1:p.Gly340= |