Linked Data
ClinVar Variation Id:
1580339
ClinVar RCV Id:
RCV002094796
dbSNP Id:
rs2148395439
MyVariant Identifiers:
chrX:g.153001648C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736194C>T , CM000685.2:g.153736194C>T | GRCh38 |
| NC_000023.10:g.153001648C>T , CM000685.1:g.153001648C>T | GRCh37 |
| NC_000023.9:g.152654842C>T | NCBI36 |
| NG_009022.2:g.16327C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1164C>T MANE Select | ENSP00000218104.3:p.Ala388= | |
| ENST00000218104.5:c.1164C>T | ENSP00000218104.3:p.Ala388= | |
| ENST00000443684.2:n.167C>T | ||
| NM_000033.3:c.1164C>T | NP_000024.2:p.Ala388= | |
| XR_938507.1:n.1580C>T | ||
| XR_938507.2:n.1580C>T | ||
| NM_000033.4:c.1164C>T MANE Select | NP_000024.2:p.Ala388= |