Linked Data
dbSNP Id:
rs781793896
ExAC:
X:53271063 A / G
gnomAD v2:
X-53271063-A-G
gnomAD v4:
X-53241881-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.53241881A>G , CM000685.2:g.53241881A>G | GRCh38 |
| NC_000023.10:g.53271063A>G , CM000685.1:g.53271063A>G | GRCh37 |
| NC_000023.9:g.53287788A>G | NCBI36 |
| NG_021296.1:g.84460T>C | |
| NG_021296.2:g.84470T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706952.1:c.3077T>C | ENSP00000516672.1:p.Val1026Ala | |
| ENST00000638521.1:c.870T>C | ||
| ENST00000638869.1:c.379T>C | ||
| ENST00000639642.1:c.208T>C | ||
| ENST00000640694.1:c.2918T>C | ENSP00000492403.1:p.Val973Ala | |
| ENST00000642864.1:c.2918T>C MANE Select | ENSP00000495726.1:p.Val973Ala | |
| ENST00000674510.1:c.2918T>C | ENSP00000502054.1:p.Val973Ala | |
| ENST00000674761.1:n.1225T>C | ||
| ENST00000675719.1:c.2888T>C | ENSP00000501927.1:p.Val963Ala | |
| ENST00000375365.2:c.2303T>C | ENSP00000364514.2:p.Val768Ala | |
| ENST00000396435.7:c.2918T>C | ENSP00000379712.3:p.Val973Ala | |
| NM_001111125.2:c.2918T>C | NP_001104595.1:p.Val973Ala | |
| NM_015075.1:c.2303T>C | NP_055890.1:p.Val768Ala | |
| XM_006724579.2:c.3014T>C | XP_006724642.1:p.Val1005Ala | |
| XM_006724580.2:c.2303T>C | XP_006724643.1:p.Val768Ala | |
| XM_006724581.2:c.3014T>C | XP_006724644.1:p.Val1005Ala | |
| XM_006724582.2:c.3014T>C | XP_006724645.1:p.Val1005Ala | |
| XM_006724583.2:c.3014T>C | XP_006724646.1:p.Val1005Ala | |
| XM_006724584.2:c.3014T>C | XP_006724647.1:p.Val1005Ala | |
| XM_011530772.1:c.2240T>C | XP_011529074.1:p.Val747Ala | |
| XM_011530773.1:c.2207T>C | XP_011529075.1:p.Val736Ala | |
| XM_011530774.1:c.3014T>C | XP_011529076.1:p.Val1005Ala | |
| XM_011530775.1:c.3014T>C | XP_011529077.1:p.Val1005Ala | |
| XM_011530776.1:c.3014T>C | XP_011529078.1:p.Val1005Ala | |
| XM_011530777.1:c.3014T>C | XP_011529079.1:p.Val1005Ala | |
| XR_938365.1:n.3241T>C | ||
| XM_006724579.3:c.3014T>C | XP_006724642.1:p.Val1005Ala | |
| XM_006724580.3:c.2303T>C | XP_006724643.1:p.Val768Ala | |
| XM_006724581.4:c.3014T>C | XP_006724644.1:p.Val1005Ala | |
| XM_006724582.4:c.3014T>C | XP_006724645.1:p.Val1005Ala | |
| XM_006724583.4:c.3014T>C | XP_006724646.1:p.Val1005Ala | |
| XM_006724584.3:c.3014T>C | XP_006724647.1:p.Val1005Ala | |
| XM_011530773.2:c.2207T>C | XP_011529075.1:p.Val736Ala | |
| XM_011530774.3:c.3014T>C | XP_011529076.1:p.Val1005Ala | |
| XM_011530776.2:c.3014T>C | XP_011529078.1:p.Val1005Ala | |
| XM_011530777.2:c.3014T>C | XP_011529079.1:p.Val1005Ala | |
| XM_017029359.2:c.2888T>C | XP_016884848.1:p.Val963Ala | |
| XM_017029360.1:c.2420T>C | XP_016884849.1:p.Val807Ala | |
| XR_938365.2:n.3235T>C | ||
| NM_001111125.3:c.2918T>C MANE Select | NP_001104595.1:p.Val973Ala | |
| NM_015075.2:c.2303T>C | NP_055890.1:p.Val768Ala |