Linked Data
dbSNP Id:
rs1210795360
gnomAD v3:
X-154772981-A-G
gnomAD v4:
X-154772981-A-G
MyVariant Identifiers:
chrX:g.154772981A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154772981A>G , CM000685.2:g.154772981A>G | GRCh38 |
| NC_000023.10:g.154001256A>G , CM000685.1:g.154001256A>G | GRCh37 |
| NC_000023.9:g.153654450A>G | NCBI36 |
| NG_009780.1:g.15226A>G , LRG_55:g.15226A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413910.6:c.917-150A>G | ENSP00000400542.2:n.917-150A>G | |
| ENST00000426673.6:c.*420-150A>G | ENSP00000407253.3:n.*420-150A>G | |
| ENST00000484317.6:n.822-150A>G | ||
| ENST00000696575.1:c.1037-150A>G | ENSP00000512730.1:n.1037-150A>G | |
| ENST00000696577.1:c.1037-150A>G | ENSP00000512731.1:n.1037-150A>G | |
| ENST00000696578.1:c.916-150A>G | ENSP00000512732.1:n.916-150A>G | |
| ENST00000696579.1:n.1139-150A>G | ||
| ENST00000696580.1:c.950-150A>G | ENSP00000512733.1:n.950-150A>G | |
| ENST00000696581.1:c.*1011-150A>G | ENSP00000512734.1:n.*1011-150A>G | |
| ENST00000696582.1:c.*243-150A>G | ENSP00000512735.1:n.*243-150A>G | |
| ENST00000696583.1:c.998-150A>G | ENSP00000512736.1:n.998-150A>G | |
| ENST00000696584.1:n.1561-150A>G | ||
| ENST00000696585.1:n.1680-150A>G | ||
| ENST00000696586.1:n.1454-150A>G | ||
| ENST00000696587.1:c.917-150A>G | ENSP00000512737.1:n.917-150A>G | |
| ENST00000696588.1:c.428-150A>G | ENSP00000513251.1:n.428-150A>G | |
| ENST00000696589.1:n.812-150A>G | ||
| ENST00000696590.1:n.661-150A>G | ||
| ENST00000696591.1:n.386-150A>G | ||
| ENST00000696592.1:n.1766A>G | ||
| ENST00000696627.1:c.1037-150A>G | ENSP00000512764.1:n.1037-150A>G | |
| ENST00000696628.1:c.1037-150A>G | ENSP00000512765.1:n.1037-150A>G | |
| ENST00000369550.10:c.1037-150A>G MANE Select | ENSP00000358563.5:n.1037-150A>G | |
| ENST00000369550.9:c.1037-150A>G | ENSP00000358563.5:n.1037-150A>G | |
| ENST00000412124.5:c.295-150A>G | ||
| ENST00000426673.5:c.397-150A>G | ||
| ENST00000475966.1:n.526-150A>G | ||
| ENST00000620277.4:c.1037-150A>G | ENSP00000478387.1:n.1037-150A>G | |
| NM_001142463.2:c.1037-150A>G | NP_001135935.1:n.1037-150A>G | |
| NM_001288747.1:c.1037-150A>G | NP_001275676.1:n.1037-150A>G | |
| NM_001363.4:c.1037-150A>G | NP_001354.1:n.1037-150A>G | |
| NR_110021.1:n.1738-150A>G | ||
| NR_110022.1:n.1857-150A>G | ||
| NR_110023.1:n.1631-150A>G | ||
| NM_001363.5:c.1037-150A>G MANE Select | NP_001354.1:n.1037-150A>G | |
| NM_001142463.3:c.1037-150A>G | NP_001135935.1:n.1037-150A>G | |
| NR_110021.2:n.1616-150A>G | ||
| NR_110022.2:n.1735-150A>G | ||
| NR_110023.2:n.1509-150A>G | ||
| NM_001288747.2:c.1037-150A>G | NP_001275676.1:n.1037-150A>G |