Linked Data
dbSNP Id:
rs1557191190
gnomAD v2:
X-153640575-A-G
gnomAD v4:
X-154412238-A-G
MyVariant Identifiers:
chrX:g.153640575A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154412238A>G , CM000685.2:g.154412238A>G | GRCh38 |
| NC_000023.10:g.153640575A>G , CM000685.1:g.153640575A>G | GRCh37 |
| NC_000023.9:g.153293769A>G | NCBI36 |
| NG_009634.1:g.5699A>G | |
| NG_012884.2:g.4851T>C | |
| NG_009634.2:g.5704A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698234.1:n.666+24A>G | ||
| ENST00000698235.1:n.225+24A>G | ||
| ENST00000698317.1:n.224A>G | ||
| ENST00000698318.1:n.85A>G | ||
| ENST00000475699.6:c.292+24A>G | ENSP00000419854.3:n.292+24A>G | |
| ENST00000476800.2:n.227A>G | ||
| ENST00000483674.3:n.129+24A>G | ||
| ENST00000601016.6:c.238+24A>G MANE Select | ENSP00000469981.1:n.238+24A>G | |
| ENST00000612012.5:c.238+24A>G | ENSP00000482070.2:n.238+24A>G | |
| ENST00000612460.5:c.238+24A>G | ENSP00000481037.1:n.238+24A>G | |
| ENST00000614595.2:n.620A>G | ||
| ENST00000615658.5:n.551+24A>G | ||
| ENST00000616020.5:c.292+24A>G | ENSP00000483636.2:n.292+24A>G | |
| ENST00000617701.5:c.238+24A>G | ENSP00000481645.1:n.238+24A>G | |
| ENST00000621647.2:n.291+24A>G | ||
| ENST00000652358.1:c.-57+286A>G | ENSP00000498464.1:n.-57+286A>G | |
| ENST00000652390.1:c.157+24A>G | ENSP00000498858.1:n.157+24A>G | |
| ENST00000652476.1:n.399+24A>G | ||
| ENST00000652682.1:c.238+24A>G | ENSP00000498288.1:n.238+24A>G | |
| ENST00000652685.1:n.290+24A>G | ||
| ENST00000369776.8:c.163+232A>G | ENSP00000358791.4:n.163+232A>G | |
| ENST00000426231.5:c.54+24A>G | ||
| ENST00000439735.2:c.238+24A>G | ENSP00000398193.1:n.238+24A>G | |
| ENST00000475699.5:c.238+24A>G | ENSP00000419854.2:n.238+24A>G | |
| ENST00000483780.5:n.12+24A>G | ||
| ENST00000601016.5:c.238+24A>G | ENSP00000469981.1:n.238+24A>G | |
| ENST00000612012.4:c.292+24A>G | ENSP00000482070.1:n.292+24A>G | |
| ENST00000612460.4:c.238+24A>G | ENSP00000481037.1:n.238+24A>G | |
| ENST00000613002.4:c.238+24A>G | ENSP00000478154.1:n.238+24A>G | |
| ENST00000613634.4:n.558+24A>G | ||
| ENST00000614595.1:n.481A>G | ||
| ENST00000615658.4:n.564+24A>G | ||
| ENST00000615986.4:c.238+24A>G | ENSP00000480133.1:n.238+24A>G | |
| ENST00000616020.4:c.292+24A>G | ENSP00000483636.1:n.292+24A>G | |
| ENST00000617701.4:c.238+24A>G | ENSP00000481645.1:n.238+24A>G | |
| ENST00000620808.4:c.238+24A>G | ENSP00000479311.1:n.238+24A>G | |
| ENST00000621647.1:n.523+24A>G | ||
| NM_000116.4:c.238+24A>G | NP_000107.1:n.238+24A>G | |
| NM_001303465.1:c.292+24A>G | NP_001290394.1:n.292+24A>G | |
| NM_181311.3:c.238+24A>G | NP_851828.1:n.238+24A>G | |
| NM_181312.3:c.238+24A>G | NP_851829.1:n.238+24A>G | |
| NM_181313.3:c.238+24A>G | NP_851830.1:n.238+24A>G | |
| NR_024048.2:n.564+24A>G | ||
| XM_006724836.1:c.292+24A>G | XP_006724899.1:n.292+24A>G | |
| XM_006724837.1:c.292+24A>G | XP_006724900.1:n.292+24A>G | |
| XM_006724839.1:c.292+24A>G | XP_006724902.1:n.292+24A>G | |
| XM_006724841.2:c.-57+24A>G | XP_006724904.1:n.-57+24A>G | |
| XM_006724842.2:c.-57+24A>G | XP_006724905.1:n.-57+24A>G | |
| XM_011531189.1:c.292+24A>G | XP_011529491.1:n.292+24A>G | |
| XM_011531190.1:c.-793A>G | XP_011529492.1:n.-793A>G | |
| XM_011531191.1:c.-775A>G | XP_011529493.1:n.-775A>G | |
| XM_011531192.1:c.-896A>G | XP_011529494.1:n.-896A>G | |
| XR_938511.1:n.595+24A>G | ||
| XM_006724841.4:c.-57+24A>G | XP_006724904.1:n.-57+24A>G | |
| XM_006724842.4:c.-57+24A>G | XP_006724905.1:n.-57+24A>G | |
| XM_011531191.2:c.-775A>G | XP_011529493.1:n.-775A>G | |
| XM_017029761.1:c.238+24A>G | XP_016885250.1:n.238+24A>G | |
| XM_017029762.1:c.292+24A>G | XP_016885251.1:n.292+24A>G | |
| XM_017029763.1:c.238+24A>G | XP_016885252.1:n.238+24A>G | |
| XM_017029765.2:c.-57+24A>G | XP_016885254.1:n.-57+24A>G | |
| XM_024452431.1:c.292+24A>G | XP_024308199.1:n.292+24A>G | |
| NM_000116.5:c.238+24A>G MANE Select | NP_000107.1:n.238+24A>G | |
| NM_001303465.2:c.292+24A>G | NP_001290394.1:n.292+24A>G | |
| NM_181311.4:c.238+24A>G | NP_851828.1:n.238+24A>G | |
| NM_181312.4:c.238+24A>G | NP_851829.1:n.238+24A>G | |
| NM_181313.4:c.238+24A>G | NP_851830.1:n.238+24A>G | |
| NR_024048.3:n.543+24A>G |