Linked Data
ClinVar Variation Id:
2085231
ClinVar RCV Id:
RCV002996167
dbSNP Id:
rs781921190
ExAC:
X:53264004 G / C
gnomAD v2:
X-53264004-G-C
gnomAD v3:
X-53234822-G-C
gnomAD v4:
X-53234822-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.53234822G>C , CM000685.2:g.53234822G>C | GRCh38 |
| NC_000023.10:g.53264004G>C , CM000685.1:g.53264004G>C | GRCh37 |
| NC_000023.9:g.53280729G>C | NCBI36 |
| NG_021296.1:g.91519C>G | |
| NG_021296.2:g.91529C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706952.1:c.4023C>G | ENSP00000516672.1:p.Pro1341= | |
| ENST00000638521.1:c.1453+961C>G | ||
| ENST00000638869.1:c.962+961C>G | ||
| ENST00000639796.1:c.316+1500C>G | ENSP00000492252.1:n.316+1500C>G | |
| ENST00000640005.1:c.514+1500C>G | ENSP00000491293.1:n.514+1500C>G | |
| ENST00000640694.1:c.*349C>G | ENSP00000492403.1:n.*349C>G | |
| ENST00000642864.1:c.3864C>G MANE Select | ENSP00000495726.1:p.Pro1288= | |
| ENST00000674510.1:c.3864C>G | ENSP00000502054.1:p.Pro1288= | |
| ENST00000675719.1:c.3834C>G | ENSP00000501927.1:p.Pro1278= | |
| ENST00000375365.2:c.*349C>G | ENSP00000364514.2:n.*349C>G | |
| ENST00000396435.7:c.3864C>G | ENSP00000379712.3:p.Pro1288= | |
| NM_001111125.2:c.3864C>G | NP_001104595.1:p.Pro1288= | |
| NM_015075.1:c.*349C>G | NP_055890.1:n.*349C>G | |
| XM_006724579.2:c.3960C>G | XP_006724642.1:p.Pro1320= | |
| XM_006724580.2:c.3249C>G | XP_006724643.1:p.Pro1083= | |
| XM_006724581.2:c.3597+961C>G | XP_006724644.1:n.3597+961C>G | |
| XM_006724582.2:c.3597+961C>G | XP_006724645.1:n.3597+961C>G | |
| XM_006724583.2:c.3547+1500C>G | XP_006724646.1:n.3547+1500C>G | |
| XM_006724584.2:c.*349C>G | XP_006724647.1:n.*349C>G | |
| XM_011530772.1:c.3186C>G | XP_011529074.1:p.Pro1062= | |
| XM_011530773.1:c.3153C>G | XP_011529075.1:p.Pro1051= | |
| XM_011530775.1:c.3547+1500C>G | XP_011529077.1:n.3547+1500C>G | |
| XM_006724579.3:c.3960C>G | XP_006724642.1:p.Pro1320= | |
| XM_006724580.3:c.3249C>G | XP_006724643.1:p.Pro1083= | |
| XM_006724581.4:c.3597+961C>G | XP_006724644.1:n.3597+961C>G | |
| XM_006724582.4:c.3597+961C>G | XP_006724645.1:n.3597+961C>G | |
| XM_006724583.4:c.3547+1500C>G | XP_006724646.1:n.3547+1500C>G | |
| XM_006724584.3:c.*349C>G | XP_006724647.1:n.*349C>G | |
| XM_011530773.2:c.3153C>G | XP_011529075.1:p.Pro1051= | |
| XM_017029359.2:c.3834C>G | XP_016884848.1:p.Pro1278= | |
| XM_017029360.1:c.3366C>G | XP_016884849.1:p.Pro1122= | |
| NM_001111125.3:c.3864C>G MANE Select | NP_001104595.1:p.Pro1288= | |
| NM_015075.2:c.*349C>G | NP_055890.1:n.*349C>G |