Linked Data
ClinVar Variation Id:
2157425
ClinVar RCV Id:
RCV003078094
dbSNP Id:
rs1557045435
gnomAD v2:
X-152959741-C-T
gnomAD v3:
X-153694286-C-T
gnomAD v4:
X-153694286-C-T
MyVariant Identifiers:
chrX:g.152959741C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153694286C>T , CM000685.2:g.153694286C>T | GRCh38 |
| NC_000023.10:g.152959741C>T , CM000685.1:g.152959741C>T | GRCh37 |
| NC_000023.9:g.152612935C>T | NCBI36 |
| NG_012016.1:g.10990C>T | |
| NG_012016.2:g.10990C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.1392+19C>T MANE Select | ENSP00000253122.5:n.1392+19C>T | |
| ENST00000253122.9:c.1392+19C>T | ENSP00000253122.5:n.1392+19C>T | |
| ENST00000413787.1:c.321+19C>T | ENSP00000400463.1:n.321+19C>T | |
| ENST00000430077.6:c.1047+19C>T | ENSP00000403041.2:n.1047+19C>T | |
| ENST00000442457.1:c.446+19C>T | ||
| ENST00000485324.1:n.1556C>T | ||
| NM_001142805.1:c.1362+19C>T | NP_001136277.1:n.1362+19C>T | |
| NM_001142806.1:c.1047+19C>T | NP_001136278.1:n.1047+19C>T | |
| NM_005629.3:c.1392+19C>T | NP_005620.1:n.1392+19C>T | |
| NM_005629.4:c.1392+19C>T MANE Select | NP_005620.1:n.1392+19C>T | |
| NM_001142805.2:c.1362+19C>T | NP_001136277.1:n.1362+19C>T |