Linked Data
MyVariant Identifiers:
chrX:g.77373590T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78118093T>C , CM000685.2:g.78118093T>C | GRCh38 |
| NC_000023.10:g.77373590T>C , CM000685.1:g.77373590T>C | GRCh37 |
| NC_000023.9:g.77260246T>C | NCBI36 |
| NG_008862.1:g.18925T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.564T>C MANE Select | ENSP00000362413.4:p.Phe188= | |
| ENST00000644362.1:c.480T>C | ENSP00000496140.1:p.Phe160= | |
| ENST00000373316.4:c.564T>C | ENSP00000362413.4:p.Phe188= | |
| ENST00000491291.1:n.556T>C | ||
| NM_000291.3:c.564T>C | NP_000282.1:p.Phe188= | |
| NM_000291.4:c.564T>C MANE Select | NP_000282.1:p.Phe188= |