Linked Data
MyVariant Identifiers:
chr9:g.12702347A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12702347A>C , CM000671.2:g.12702347A>C | GRCh38 |
| NC_000009.11:g.12702347A>C , CM000671.1:g.12702347A>C | GRCh37 |
| NC_000009.10:g.12692347A>C | NCBI36 |
| NG_011705.1:g.13962A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.990A>C (TYRP1) MANE Select | ENSP00000373570.4:p.Pro330= | |
| ENST00000381136.2:c.120A>C (TYRP1) | ENSP00000370528.2:p.Pro40= | |
| ENST00000381142.3:n.227A>C (TYRP1) | ||
| ENST00000388918.9:c.990A>C (TYRP1) | ENSP00000373570.4:p.Pro330= | |
| ENST00000470909.1:n.248A>C (TYRP1) | ||
| NM_000550.2:c.990A>C (TYRP1) | NP_000541.1:p.Pro330= | |
| NR_125775.1:n.317-1721T>G (LURAP1L-AS1) | ||
| XR_001746372.2:n.974A>C (TYRP1) | ||
| NM_000550.3:c.990A>C (TYRP1) MANE Select | NP_000541.1:p.Pro330= |