Linked Data
dbSNP Id:
rs1269723577
gnomAD v3:
X-153770263-G-T
gnomAD v4:
X-153770263-G-T
MyVariant Identifiers:
chrX:g.153770263G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153770263G>T , CM000685.2:g.153770263G>T | GRCh38 |
| NC_000023.10:g.153035718G>T , CM000685.1:g.153035718G>T | GRCh37 |
| NC_000023.9:g.152688912G>T | NCBI36 |
| NG_013255.1:g.11068G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361971.10:c.1786+15G>T MANE Select | ENSP00000355378.5:n.1786+15G>T | |
| ENST00000361971.9:c.1786+15G>T | ENSP00000355378.5:n.1786+15G>T | |
| ENST00000538966.5:c.1855+15G>T | ENSP00000442736.1:n.1855+15G>T | |
| NM_001163257.1:c.1855+15G>T | NP_001156729.1:n.1855+15G>T | |
| NM_005393.2:c.1786+15G>T | NP_005384.2:n.1786+15G>T | |
| NM_005393.3:c.1786+15G>T MANE Select | NP_005384.2:n.1786+15G>T | |
| NM_001163257.2:c.1855+15G>T | NP_001156729.1:n.1855+15G>T |