dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12710090T>A , CM000671.2:g.12710090T>A | GRCh38 |
| NC_000009.11:g.12710090T>A , CM000671.1:g.12710090T>A | GRCh37 |
| NC_000009.10:g.12700090T>A | NCBI36 |
| NG_011705.1:g.21705T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.*908T>A (TYRP1) MANE Select | ENSP00000373570.4:n.*908T>A | |
| ENST00000388918.9:c.*908T>A (TYRP1) | ENSP00000373570.4:n.*908T>A | |
| NM_000550.2:c.*908T>A (TYRP1) | NP_000541.1:n.*908T>A | |
| NR_125775.1:n.317-9464A>T (LURAP1L-AS1) | ||
| NM_000550.3:c.*908T>A (TYRP1) MANE Select | NP_000541.1:n.*908T>A |