Linked Data
MyVariant Identifiers:
chrX:g.49957174C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50192523C>A , CM000685.2:g.50192523C>A | GRCh38 |
| NC_000023.10:g.49957174C>A , CM000685.1:g.49957174C>A | GRCh37 |
| NC_000023.9:g.49843914C>A | NCBI36 |
| NG_012552.1:g.13491G>T | |
| NG_012552.2:g.13491G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358526.7:c.2190G>T MANE Select | ENSP00000351327.2:p.Ser730= | |
| ENST00000358526.6:c.2190G>T | ENSP00000351327.2:p.Ser730= | |
| ENST00000376064.7:c.2163G>T | ENSP00000365232.3:p.Ser721= | |
| ENST00000481402.5:n.2302G>T | ||
| NM_003886.2:c.2190G>T | NP_003877.2:p.Ser730= | |
| NM_139289.1:c.2163G>T | NP_647450.1:p.Ser721= | |
| NM_003886.3:c.2190G>T MANE Select | NP_003877.2:p.Ser730= | |
| NM_139289.2:c.2163G>T | NP_647450.1:p.Ser721= |