Linked Data
MyVariant Identifiers:
chrX:g.150345866G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.151177394G>C , CM000685.2:g.151177394G>C | GRCh38 |
| NC_000023.10:g.150345866G>C , CM000685.1:g.150345866G>C | GRCh37 |
| NC_000023.9:g.150096524G>C | NCBI36 |
| NG_016405.1:g.5811G>C | |
| NG_016405.2:g.5811G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218316.4:c.187+486G>C (GPR50) MANE Select | ENSP00000218316.3:n.187+486G>C | |
| ENST00000218316.3:c.187+486G>C (GPR50) | ENSP00000218316.3:n.187+486G>C | |
| ENST00000617907.1:c.187+486G>C (GPR50) | ENSP00000484496.1:n.187+486G>C | |
| NM_004224.3:c.187+486G>C (GPR50) MANE Select | NP_004215.2:n.187+486G>C | |
| NR_135300.1:n.443C>G (GPR50-AS1) |