Linked Data
MyVariant Identifiers:
chrX:g.153001882G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736428G>A , CM000685.2:g.153736428G>A | GRCh38 |
| NC_000023.10:g.153001882G>A , CM000685.1:g.153001882G>A | GRCh37 |
| NC_000023.9:g.152655076G>A | NCBI36 |
| NG_009022.2:g.16561G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1308G>A MANE Select | ENSP00000218104.3:p.Arg436= | |
| ENST00000218104.5:c.1308G>A | ENSP00000218104.3:p.Arg436= | |
| ENST00000443684.2:n.311G>A | ||
| NM_000033.3:c.1308G>A | NP_000024.2:p.Arg436= | |
| XR_938507.1:n.1724G>A | ||
| XR_938507.2:n.1724G>A | ||
| NM_000033.4:c.1308G>A MANE Select | NP_000024.2:p.Arg436= |