Linked Data
MyVariant Identifiers:
chrX:g.77369289C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78113792C>T , CM000685.2:g.78113792C>T | GRCh38 |
| NC_000023.10:g.77369289C>T , CM000685.1:g.77369289C>T | GRCh37 |
| NC_000023.9:g.77255945C>T | NCBI36 |
| NG_008862.1:g.14624C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.165C>T MANE Select | ENSP00000362413.4:p.Ala55= | |
| ENST00000644362.1:c.81C>T | ENSP00000496140.1:p.Ala27= | |
| ENST00000373316.4:c.165C>T | ENSP00000362413.4:p.Ala55= | |
| ENST00000477335.5:n.301C>T | ||
| ENST00000491291.1:n.157C>T | ||
| NM_000291.3:c.165C>T | NP_000282.1:p.Ala55= | |
| NM_000291.4:c.165C>T MANE Select | NP_000282.1:p.Ala55= |