Linked Data
MyVariant Identifiers:
chrX:g.153006040T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153740586T>C , CM000685.2:g.153740586T>C | GRCh38 |
| NC_000023.10:g.153006040T>C , CM000685.1:g.153006040T>C | GRCh37 |
| NC_000023.9:g.152659234T>C | NCBI36 |
| NG_009022.2:g.20719T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1647T>C MANE Select | ENSP00000218104.3:p.Ser549= | |
| ENST00000218104.5:c.1647T>C | ENSP00000218104.3:p.Ser549= | |
| ENST00000443684.2:n.650T>C | ||
| NM_000033.3:c.1647T>C | NP_000024.2:p.Ser549= | |
| XR_938507.1:n.2119T>C | ||
| XR_938507.2:n.2119T>C | ||
| NM_000033.4:c.1647T>C MANE Select | NP_000024.2:p.Ser549= |