Linked Data
dbSNP Id:
rs1298610666
gnomAD v3:
X-152867370-A-G
gnomAD v4:
X-152867370-A-G
MyVariant Identifiers:
chrX:g.152867370A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.152867370A>G , CM000685.2:g.152867370A>G | GRCh38 |
| NC_000023.10:g.152035914A>G , CM000685.1:g.152035914A>G | GRCh37 |
| NC_000023.9:g.151786570A>G | NCBI36 |
| NG_009163.1:g.41404A>G | |
| NG_009163.2:g.41404A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370274.8:c.687-201A>G MANE Select | ENSP00000359297.3:n.687-201A>G | |
| ENST00000370274.7:c.687-201A>G | ENSP00000359297.3:n.687-201A>G | |
| ENST00000432467.1:c.687-201A>G | ENSP00000396266.1:n.687-201A>G | |
| ENST00000440023.5:c.687-201A>G | ENSP00000391854.1:n.687-201A>G | |
| NM_001129765.1:c.687-201A>G | NP_001123237.1:n.687-201A>G | |
| NM_015922.2:c.687-201A>G | NP_057006.1:n.687-201A>G | |
| XM_011531178.1:c.687-201A>G | XP_011529480.1:n.687-201A>G | |
| XM_011531178.2:c.687-201A>G | XP_011529480.1:n.687-201A>G | |
| XM_017029564.1:c.735-201A>G | XP_016885053.1:n.735-201A>G | |
| NM_015922.3:c.687-201A>G MANE Select | NP_057006.1:n.687-201A>G | |
| NM_001129765.2:c.687-201A>G | NP_001123237.1:n.687-201A>G |