Linked Data
dbSNP Id:
rs781868535
ExAC:
X:53277453 T / C
gnomAD v2:
X-53277453-T-C
gnomAD v4:
X-53248271-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.53248271T>C , CM000685.2:g.53248271T>C | GRCh38 |
| NC_000023.10:g.53277453T>C , CM000685.1:g.53277453T>C | GRCh37 |
| NC_000023.9:g.53294178T>C | NCBI36 |
| NG_021296.1:g.78070A>G | |
| NG_021296.2:g.78080A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706952.1:c.2619-35A>G | ENSP00000516672.1:n.2619-35A>G | |
| ENST00000638521.1:c.412-35A>G | ||
| ENST00000640694.1:c.2460-35A>G | ENSP00000492403.1:n.2460-35A>G | |
| ENST00000642864.1:c.2460-35A>G MANE Select | ENSP00000495726.1:n.2460-35A>G | |
| ENST00000674510.1:c.2460-35A>G | ENSP00000502054.1:n.2460-35A>G | |
| ENST00000674761.1:n.176A>G | ||
| ENST00000675719.1:c.2430-35A>G | ENSP00000501927.1:n.2430-35A>G | |
| ENST00000375365.2:c.1845-35A>G | ENSP00000364514.2:n.1845-35A>G | |
| ENST00000396435.7:c.2460-35A>G | ENSP00000379712.3:n.2460-35A>G | |
| NM_001111125.2:c.2460-35A>G | NP_001104595.1:n.2460-35A>G | |
| NM_015075.1:c.1845-35A>G | NP_055890.1:n.1845-35A>G | |
| XM_006724579.2:c.2556-35A>G | XP_006724642.1:n.2556-35A>G | |
| XM_006724580.2:c.1845-35A>G | XP_006724643.1:n.1845-35A>G | |
| XM_006724581.2:c.2556-35A>G | XP_006724644.1:n.2556-35A>G | |
| XM_006724582.2:c.2556-35A>G | XP_006724645.1:n.2556-35A>G | |
| XM_006724583.2:c.2556-35A>G | XP_006724646.1:n.2556-35A>G | |
| XM_006724584.2:c.2556-35A>G | XP_006724647.1:n.2556-35A>G | |
| XM_011530772.1:c.1782-35A>G | XP_011529074.1:n.1782-35A>G | |
| XM_011530773.1:c.1749-35A>G | XP_011529075.1:n.1749-35A>G | |
| XM_011530774.1:c.2556-35A>G | XP_011529076.1:n.2556-35A>G | |
| XM_011530775.1:c.2556-35A>G | XP_011529077.1:n.2556-35A>G | |
| XM_011530776.1:c.2556-35A>G | XP_011529078.1:n.2556-35A>G | |
| XM_011530777.1:c.2556-35A>G | XP_011529079.1:n.2556-35A>G | |
| XR_938365.1:n.2783-35A>G | ||
| XM_006724579.3:c.2556-35A>G | XP_006724642.1:n.2556-35A>G | |
| XM_006724580.3:c.1845-35A>G | XP_006724643.1:n.1845-35A>G | |
| XM_006724581.4:c.2556-35A>G | XP_006724644.1:n.2556-35A>G | |
| XM_006724582.4:c.2556-35A>G | XP_006724645.1:n.2556-35A>G | |
| XM_006724583.4:c.2556-35A>G | XP_006724646.1:n.2556-35A>G | |
| XM_006724584.3:c.2556-35A>G | XP_006724647.1:n.2556-35A>G | |
| XM_011530773.2:c.1749-35A>G | XP_011529075.1:n.1749-35A>G | |
| XM_011530774.3:c.2556-35A>G | XP_011529076.1:n.2556-35A>G | |
| XM_011530776.2:c.2556-35A>G | XP_011529078.1:n.2556-35A>G | |
| XM_011530777.2:c.2556-35A>G | XP_011529079.1:n.2556-35A>G | |
| XM_017029359.2:c.2430-35A>G | XP_016884848.1:n.2430-35A>G | |
| XM_017029360.1:c.1962-35A>G | XP_016884849.1:n.1962-35A>G | |
| XR_938365.2:n.2777-35A>G | ||
| NM_001111125.3:c.2460-35A>G MANE Select | NP_001104595.1:n.2460-35A>G | |
| NM_015075.2:c.1845-35A>G | NP_055890.1:n.1845-35A>G |