Linked Data
ClinVar Variation Id:
459936
dbSNP Id:
rs61760965
ExAC:
13:101101556 A / G
gnomAD v2:
13-101101556-A-G
gnomAD v3:
13-100449302-A-G
gnomAD v4:
13-100449302-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.100449302A>G , CM000675.2:g.100449302A>G | GRCh38 |
| NC_000013.10:g.101101556A>G , CM000675.1:g.101101556A>G | GRCh37 |
| NC_000013.9:g.99899557A>G | NCBI36 |
| NG_008768.1:g.365220A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376285.6:c.1896A>G MANE Select | ENSP00000365462.1:p.Thr632= | |
| ENST00000636366.1:c.1094A>G | ||
| ENST00000636475.1:c.1411A>G | ||
| ENST00000637657.1:c.1556A>G | ||
| ENST00000647303.1:c.*1380A>G | ENSP00000495663.1:n.*1380A>G | |
| ENST00000376279.7:c.1896A>G | ENSP00000365456.3:p.Thr632= | |
| ENST00000376285.5:c.1896A>G | ENSP00000365462.1:p.Thr632= | |
| ENST00000376286.8:c.1818A>G | ENSP00000365463.4:p.Thr606= | |
| ENST00000413170.1:c.226A>G | ||
| ENST00000458283.5:c.253A>G | ||
| NM_000282.3:c.1896A>G | NP_000273.2:p.Thr632= | |
| NM_001127692.2:c.1818A>G | NP_001121164.1:p.Thr606= | |
| NM_001178004.1:c.1896A>G | NP_001171475.1:p.Thr632= | |
| XM_005254059.2:c.1896A>G | XP_005254116.1:p.Thr632= | |
| XM_011521093.1:c.1896A>G | XP_011519395.1:p.Thr632= | |
| XR_931615.1:n.1894A>G | ||
| NM_001352605.1:c.1845+23571A>G | NP_001339534.1:n.1845+23571A>G | |
| NM_001352606.1:c.1752A>G | NP_001339535.1:p.Thr584= | |
| NM_001352607.1:c.1818A>G | NP_001339536.1:p.Thr606= | |
| NM_001352608.1:c.1674A>G | NP_001339537.1:p.Thr558= | |
| NM_001352609.1:c.1896A>G | NP_001339538.1:p.Thr632= | |
| NM_001352610.1:c.951A>G | NP_001339539.1:p.Thr317= | |
| NM_001352611.1:c.900+23571A>G | NP_001339540.1:n.900+23571A>G | |
| NM_001352612.1:c.807A>G | NP_001339541.1:p.Thr269= | |
| NR_148027.1:n.2086A>G | ||
| NR_148028.1:n.1983A>G | ||
| NR_148029.1:n.1905A>G | ||
| NR_148030.1:n.2086A>G | ||
| NR_148031.1:n.1899A>G | ||
| XM_017020605.1:c.1975A>G | XP_016876094.1:p.Ser659Gly | |
| XM_017020606.1:c.1897A>G | XP_016876095.1:p.Ser633Gly | |
| XM_017020607.1:c.1876A>G | XP_016876096.1:p.Ser626Gly | |
| XM_017020609.1:c.1797A>G | XP_016876098.1:p.Thr599= | |
| XM_017020611.1:c.1975A>G | XP_016876100.1:p.Ser659Gly | |
| XM_017020612.1:c.1975A>G | XP_016876101.1:p.Ser659Gly | |
| XM_017020613.1:c.1975A>G | XP_016876102.1:p.Ser659Gly | |
| XR_001749567.1:n.2076A>G | ||
| XR_001749568.1:n.2163A>G | ||
| XR_001749569.1:n.2163A>G | ||
| XR_001749574.1:n.1932A>G | ||
| XR_001749576.1:n.1633A>G | ||
| XR_001749577.1:n.1530A>G | ||
| NM_000282.4:c.1896A>G MANE Select | NP_000273.2:p.Thr632= | |
| NM_001352605.2:c.1845+23571A>G | NP_001339534.1:n.1845+23571A>G | |
| NM_001352606.2:c.1752A>G | NP_001339535.1:p.Thr584= | |
| NM_001352607.2:c.1818A>G | NP_001339536.1:p.Thr606= | |
| NM_001352608.2:c.1674A>G | NP_001339537.1:p.Thr558= | |
| NM_001352609.2:c.1896A>G | NP_001339538.1:p.Thr632= | |
| NM_001352610.2:c.951A>G | NP_001339539.1:p.Thr317= | |
| NM_001352611.2:c.900+23571A>G | NP_001339540.1:n.900+23571A>G | |
| NM_001352612.2:c.807A>G | NP_001339541.1:p.Thr269= | |
| NR_148027.2:n.2008A>G | ||
| NR_148028.2:n.1905A>G | ||
| NR_148029.2:n.1827A>G | ||
| NR_148030.2:n.2008A>G | ||
| NR_148031.2:n.1821A>G | ||
| NM_001127692.3:c.1818A>G | NP_001121164.1:p.Thr606= | |
| NM_001178004.2:c.1896A>G | NP_001171475.1:p.Thr632= |