Linked Data
ClinVar Variation Id:
2805444
ClinVar RCV Id:
RCV003676759
COSMIC:
COSM25572
MyVariant Identifiers:
chrX:g.73960792G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74740957G>A , CM000685.2:g.74740957G>A | GRCh38 |
| NC_000023.10:g.73960792G>A , CM000685.1:g.73960792G>A | GRCh37 |
| NC_000023.9:g.73877517G>A | NCBI36 |
| NG_027726.1:g.189496C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000055682.12:c.3600C>T MANE Select | ENSP00000055682.5:p.Ser1200= | |
| ENST00000616200.2:c.3600C>T | ENSP00000480284.1:p.Ser1200= | |
| ENST00000642681.2:c.3600C>T | ENSP00000495800.1:p.Ser1200= | |
| ENST00000055682.10:c.3600C>T | ENSP00000055682.5:p.Ser1200= | |
| ENST00000616200.1:c.3600C>T | ENSP00000480284.1:p.Ser1200= | |
| NM_001008537.2:c.3600C>T | NP_001008537.1:p.Ser1200= | |
| XM_011530935.1:c.3600C>T | XP_011529237.1:p.Ser1200= | |
| NM_001008537.3:c.3600C>T MANE Select | NP_001008537.1:p.Ser1200= |