Linked Data
ClinVar Variation Id:
1111651
ClinVar RCV Id:
RCV001438318
dbSNP Id:
rs1440978011
MyVariant Identifiers:
chrX:g.153736262del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736262del , CM000685.2:g.153736262del | GRCh38 |
| NC_000023.10:g.153001716del , CM000685.1:g.153001716del | GRCh37 |
| NC_000023.9:g.152654910del | NCBI36 |
| NG_009022.2:g.16395del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1224+8del MANE Select | ENSP00000218104.3:n.1224+8del | |
| ENST00000218104.5:c.1224+8del | ENSP00000218104.3:n.1224+8del | |
| ENST00000443684.2:n.227+8del | ||
| NM_000033.3:c.1224+8del | NP_000024.2:n.1224+8del | |
| XR_938507.1:n.1640+8del | ||
| XR_938507.2:n.1640+8del | ||
| NM_000033.4:c.1224+8del MANE Select | NP_000024.2:n.1224+8del |