Linked Data
MyVariant Identifiers:
chr9:g.12702272C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12702272C>T , CM000671.2:g.12702272C>T | GRCh38 |
| NC_000009.11:g.12702272C>T , CM000671.1:g.12702272C>T | GRCh37 |
| NC_000009.10:g.12692272C>T | NCBI36 |
| NG_011705.1:g.13887C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.915C>T (TYRP1) MANE Select | ENSP00000373570.4:p.Ser305= | |
| ENST00000381136.2:c.45C>T (TYRP1) | ENSP00000370528.2:p.Gly15= | |
| ENST00000381142.3:n.152C>T (TYRP1) | ||
| ENST00000388918.9:c.915C>T (TYRP1) | ENSP00000373570.4:p.Ser305= | |
| ENST00000470909.1:n.173C>T (TYRP1) | ||
| NM_000550.2:c.915C>T (TYRP1) | NP_000541.1:p.Ser305= | |
| NR_125775.1:n.317-1646G>A (LURAP1L-AS1) | ||
| XR_001746372.2:n.899C>T (TYRP1) | ||
| NM_000550.3:c.915C>T (TYRP1) MANE Select | NP_000541.1:p.Ser305= |