Linked Data
MyVariant Identifiers:
chrX:g.100601543G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101346555G>T , CM000685.2:g.101346555G>T | GRCh38 |
| NC_000023.10:g.100601543G>T , CM000685.1:g.100601543G>T | GRCh37 |
| NC_000023.9:g.100488199G>T | NCBI36 |
| NG_011734.1:g.7415C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.4:c.238C>A MANE Select | ENSP00000361993.3:p.Arg80= | |
| ENST00000644112.2:c.*1832C>A | ENSP00000494385.1:n.*1832C>A | |
| ENST00000645279.1:c.*432C>A | ENSP00000494239.1:n.*432C>A | |
| ENST00000647480.1:n.755C>A | ||
| ENST00000372902.3:c.238C>A | ENSP00000361993.3:p.Arg80= | |
| NM_004085.3:c.238C>A | NP_004076.1:p.Arg80= | |
| NM_004085.4:c.238C>A MANE Select | NP_004076.1:p.Arg80= | |
| NM_001145951.2:c.*1832C>A | NP_001139423.1:n.*1832C>A |