Linked Data
ClinVar Variation Id:
728780
ClinVar RCV Id:
RCV000903322
dbSNP Id:
rs543352333
ExAC:
13:100921045 T / A
gnomAD v2:
13-100921045-T-A
gnomAD v3:
13-100268791-T-A
gnomAD v4:
13-100268791-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.100268791T>A , CM000675.2:g.100268791T>A | GRCh38 |
| NC_000013.10:g.100921045T>A , CM000675.1:g.100921045T>A | GRCh37 |
| NC_000013.9:g.99719046T>A | NCBI36 |
| NG_008768.1:g.184709T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376285.6:c.914+8T>A MANE Select | ENSP00000365462.1:n.914+8T>A | |
| ENST00000636366.1:c.793+8T>A | ||
| ENST00000636420.1:c.793+8T>A | ||
| ENST00000636475.1:c.793+8T>A | ||
| ENST00000637657.1:c.793+8T>A | ||
| ENST00000647303.1:c.*762+8T>A | ENSP00000495663.1:n.*762+8T>A | |
| ENST00000376279.7:c.914+8T>A | ENSP00000365456.3:n.914+8T>A | |
| ENST00000376285.5:c.914+8T>A | ENSP00000365462.1:n.914+8T>A | |
| ENST00000376286.8:c.836+8T>A | ENSP00000365463.4:n.836+8T>A | |
| NM_000282.3:c.914+8T>A | NP_000273.2:n.914+8T>A | |
| NM_001127692.2:c.836+8T>A | NP_001121164.1:n.836+8T>A | |
| NM_001178004.1:c.914+8T>A | NP_001171475.1:n.914+8T>A | |
| XM_005254059.2:c.914+8T>A | XP_005254116.1:n.914+8T>A | |
| XM_011521093.1:c.914+8T>A | XP_011519395.1:n.914+8T>A | |
| XR_931615.1:n.1015+8T>A | ||
| XR_931616.1:n.1015+8T>A | ||
| NM_001352605.1:c.914+8T>A | NP_001339534.1:n.914+8T>A | |
| NM_001352606.1:c.914+8T>A | NP_001339535.1:n.914+8T>A | |
| NM_001352607.1:c.836+8T>A | NP_001339536.1:n.836+8T>A | |
| NM_001352608.1:c.836+8T>A | NP_001339537.1:n.836+8T>A | |
| NM_001352609.1:c.914+8T>A | NP_001339538.1:n.914+8T>A | |
| NM_001352610.1:c.-32+8T>A | NP_001339539.1:n.-32+8T>A | |
| NM_001352611.1:c.-32+8T>A | NP_001339540.1:n.-32+8T>A | |
| NM_001352612.1:c.-32+8T>A | NP_001339541.1:n.-32+8T>A | |
| NR_148027.1:n.1020+8T>A | ||
| NR_148028.1:n.1020+8T>A | ||
| NR_148029.1:n.942+8T>A | ||
| NR_148030.1:n.1020+8T>A | ||
| NR_148031.1:n.1020+8T>A | ||
| XM_017020605.1:c.914+8T>A | XP_016876094.1:n.914+8T>A | |
| XM_017020606.1:c.836+8T>A | XP_016876095.1:n.836+8T>A | |
| XM_017020607.1:c.815+8T>A | XP_016876096.1:n.815+8T>A | |
| XM_017020609.1:c.815+8T>A | XP_016876098.1:n.815+8T>A | |
| XM_017020611.1:c.914+8T>A | XP_016876100.1:n.914+8T>A | |
| XM_017020612.1:c.914+8T>A | XP_016876101.1:n.914+8T>A | |
| XM_017020613.1:c.914+8T>A | XP_016876102.1:n.914+8T>A | |
| XM_017020615.1:c.914+8T>A | XP_016876104.1:n.914+8T>A | |
| XM_017020616.1:c.914+8T>A | XP_016876105.1:n.914+8T>A | |
| XR_001749567.1:n.1015+8T>A | ||
| XR_001749568.1:n.1015+8T>A | ||
| XR_001749569.1:n.1015+8T>A | ||
| XR_001749574.1:n.866+8T>A | ||
| XR_001749576.1:n.1015+8T>A | ||
| XR_001749577.1:n.1015+8T>A | ||
| NM_000282.4:c.914+8T>A MANE Select | NP_000273.2:n.914+8T>A | |
| NM_001352605.2:c.914+8T>A | NP_001339534.1:n.914+8T>A | |
| NM_001352606.2:c.914+8T>A | NP_001339535.1:n.914+8T>A | |
| NM_001352607.2:c.836+8T>A | NP_001339536.1:n.836+8T>A | |
| NM_001352608.2:c.836+8T>A | NP_001339537.1:n.836+8T>A | |
| NM_001352609.2:c.914+8T>A | NP_001339538.1:n.914+8T>A | |
| NM_001352610.2:c.-32+8T>A | NP_001339539.1:n.-32+8T>A | |
| NM_001352611.2:c.-32+8T>A | NP_001339540.1:n.-32+8T>A | |
| NM_001352612.2:c.-32+8T>A | NP_001339541.1:n.-32+8T>A | |
| NR_148027.2:n.942+8T>A | ||
| NR_148028.2:n.942+8T>A | ||
| NR_148029.2:n.864+8T>A | ||
| NR_148030.2:n.942+8T>A | ||
| NR_148031.2:n.942+8T>A | ||
| NM_001127692.3:c.836+8T>A | NP_001121164.1:n.836+8T>A | |
| NM_001178004.2:c.914+8T>A | NP_001171475.1:n.914+8T>A |