Linked Data
ClinVar Variation Id:
1622985
ClinVar RCV Id:
RCV002108680
dbSNP Id:
rs1178252669
gnomAD v2:
9-13110069-C-T
gnomAD v3:
9-13110070-C-T
gnomAD v4:
9-13110070-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.13110070C>T , CM000671.2:g.13110070C>T | GRCh38 |
| NC_000009.11:g.13110069C>T , CM000671.1:g.13110069C>T | GRCh37 |
| NC_000009.10:g.13100069C>T | NCBI36 |
| NG_042810.1:g.174495G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319217.12:c.5830-6G>A MANE Select | ENSP00000320006.7:n.5830-6G>A | |
| ENST00000447879.6:c.5731-6G>A | ENSP00000415208.1:n.5731-6G>A | |
| ENST00000319198.10:n.2330-6G>A | ||
| ENST00000319217.11:c.5830-6G>A | ENSP00000320006.7:n.5830-6G>A | |
| ENST00000381017.6:n.1390-6G>A | ||
| ENST00000381022.6:c.5731-6G>A | ENSP00000370410.3:n.5731-6G>A | |
| ENST00000438511.5:c.1453-6G>A | ENSP00000415964.1:n.1453-6G>A | |
| ENST00000447879.5:c.5731-6G>A | ENSP00000415208.1:n.5731-6G>A | |
| ENST00000536827.5:c.5644-6G>A | ENSP00000444151.1:n.5644-6G>A | |
| ENST00000538841.5:c.2407-6G>A | ENSP00000444717.1:n.2407-6G>A | |
| ENST00000539508.5:n.5717-6G>A | ||
| ENST00000541718.5:c.5743-6G>A | ENSP00000439807.1:n.5743-6G>A | |
| ENST00000542806.5:c.1968-6G>A | ||
| ENST00000545857.5:c.2638-6G>A | ENSP00000444230.1:n.2638-6G>A | |
| ENST00000546205.5:c.5872-6G>A | ENSP00000446358.1:n.5872-6G>A | |
| NM_001261406.1:c.5731-6G>A | NP_001248335.1:n.5731-6G>A | |
| NM_001261407.1:c.5644-6G>A | NP_001248336.1:n.5644-6G>A | |
| NM_003829.4:c.5743-6G>A | NP_003820.2:n.5743-6G>A | |
| XM_005251622.3:c.5830-6G>A | XP_005251679.1:n.5830-6G>A | |
| XM_005251623.3:c.5620-6G>A | XP_005251680.1:n.5620-6G>A | |
| XM_006716885.2:c.5830-6G>A | XP_006716948.1:n.5830-6G>A | |
| XM_006716886.2:c.5830-6G>A | XP_006716949.1:n.5830-6G>A | |
| XM_006716887.2:c.5830-6G>A | XP_006716950.1:n.5830-6G>A | |
| XM_006716888.2:c.5743-6G>A | XP_006716951.1:n.5743-6G>A | |
| XM_006716889.2:c.5731-6G>A | XP_006716952.1:n.5731-6G>A | |
| XM_006716890.2:c.5713-6G>A | XP_006716953.1:n.5713-6G>A | |
| XM_006716891.2:c.5644-6G>A | XP_006716954.1:n.5644-6G>A | |
| NM_001330637.1:c.5830-6G>A | NP_001317566.1:n.5830-6G>A | |
| XM_005251623.4:c.5620-6G>A | XP_005251680.1:n.5620-6G>A | |
| XM_006716885.3:c.5830-6G>A | XP_006716948.1:n.5830-6G>A | |
| XM_006716886.3:c.5830-6G>A | XP_006716949.1:n.5830-6G>A | |
| XM_006716887.4:c.5830-6G>A | XP_006716950.1:n.5830-6G>A | |
| XM_006716888.3:c.5743-6G>A | XP_006716951.1:n.5743-6G>A | |
| XM_006716889.3:c.5731-6G>A | XP_006716952.1:n.5731-6G>A | |
| XM_006716891.3:c.5644-6G>A | XP_006716954.1:n.5644-6G>A | |
| XM_017015252.1:c.5746-6G>A | XP_016870741.1:n.5746-6G>A | |
| XM_017015253.1:c.5644-6G>A | XP_016870742.1:n.5644-6G>A | |
| XM_017015254.1:c.5620-6G>A | XP_016870743.1:n.5620-6G>A | |
| XM_017015255.1:c.5620-6G>A | XP_016870744.1:n.5620-6G>A | |
| XM_017015256.1:c.5533-6G>A | XP_016870745.1:n.5533-6G>A | |
| XM_017015257.1:c.5533-6G>A | XP_016870746.1:n.5533-6G>A | |
| XM_024447708.1:c.5830-6G>A | XP_024303476.1:n.5830-6G>A | |
| XR_002956817.1:n.8860-6G>A | ||
| NM_001261406.2:c.5731-6G>A | NP_001248335.1:n.5731-6G>A | |
| NM_001261407.2:c.5644-6G>A | NP_001248336.1:n.5644-6G>A | |
| NM_001330637.2:c.5830-6G>A | NP_001317566.1:n.5830-6G>A | |
| NM_001375413.1:c.5929-6G>A | NP_001362342.1:n.5929-6G>A | |
| NM_001375416.1:c.5731-6G>A | NP_001362345.1:n.5731-6G>A | |
| NM_001375417.1:c.5731-6G>A | NP_001362346.1:n.5731-6G>A | |
| NM_001375418.1:c.5731-6G>A | NP_001362347.1:n.5731-6G>A | |
| NM_001375419.1:c.5644-6G>A | NP_001362348.1:n.5644-6G>A | |
| NM_001375420.1:c.5620-6G>A | NP_001362349.1:n.5620-6G>A | |
| NM_001375421.1:c.5620-6G>A | NP_001362350.1:n.5620-6G>A | |
| NM_001375422.1:c.5620-6G>A | NP_001362351.1:n.5620-6G>A | |
| NM_001375423.1:c.5620-6G>A | NP_001362352.1:n.5620-6G>A | |
| NM_001375424.1:c.5620-6G>A | NP_001362353.1:n.5620-6G>A | |
| NM_001375425.1:c.5533-6G>A | NP_001362354.1:n.5533-6G>A | |
| NM_001375426.1:c.5533-6G>A | NP_001362355.1:n.5533-6G>A | |
| NM_001375427.1:c.5422-6G>A | NP_001362356.1:n.5422-6G>A | |
| NM_003829.5:c.5743-6G>A | NP_003820.2:n.5743-6G>A | |
| NM_001378778.1:c.5830-6G>A MANE Select | NP_001365707.1:n.5830-6G>A |