Linked Data
dbSNP Id:
rs758091663
ExAC:
6:52344616 C / T
gnomAD v2:
6-52344616-C-T
gnomAD v3:
6-52479818-C-T
gnomAD v4:
6-52479818-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.52479818C>T , CM000668.2:g.52479818C>T | GRCh38 |
| NC_000006.11:g.52344616C>T , CM000668.1:g.52344616C>T | GRCh37 |
| NC_000006.10:g.52452575C>T | NCBI36 |
| NG_016760.1:g.64623C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371068.11:c.1640+31C>T MANE Select | ENSP00000360107.4:n.1640+31C>T | |
| ENST00000480623.6:c.1640+31C>T | ENSP00000434498.2:n.1640+31C>T | |
| ENST00000635760.1:c.1316+31C>T | ENSP00000489765.1:n.1316+31C>T | |
| ENST00000635812.1:c.*941+31C>T | ENSP00000490859.1:n.*941+31C>T | |
| ENST00000635866.1:c.*1509+31C>T | ENSP00000489866.1:n.*1509+31C>T | |
| ENST00000635911.1:n.3158+31C>T | ||
| ENST00000635984.1:c.1316+31C>T | ENSP00000489921.1:n.1316+31C>T | |
| ENST00000635996.1:c.1640+31C>T | ENSP00000490256.1:n.1640+31C>T | |
| ENST00000636107.1:c.1640+31C>T | ENSP00000489680.1:n.1640+31C>T | |
| ENST00000636311.1:n.1534+31C>T | ||
| ENST00000636343.1:c.1306+31C>T | ||
| ENST00000636379.1:c.1352+31C>T | ENSP00000490622.1:n.1352+31C>T | |
| ENST00000636398.1:c.1340+31C>T | ENSP00000489654.1:n.1340+31C>T | |
| ENST00000636489.1:c.1583+31C>T | ENSP00000489998.1:n.1583+31C>T | |
| ENST00000636616.1:n.1201+31C>T | ||
| ENST00000636702.1:c.1610+31C>T | ENSP00000489623.1:n.1610+31C>T | |
| ENST00000636954.1:c.1583+31C>T | ENSP00000489966.1:n.1583+31C>T | |
| ENST00000637089.1:c.1640+31C>T | ENSP00000489854.1:n.1640+31C>T | |
| ENST00000637121.1:n.1442+31C>T | ||
| ENST00000637263.1:c.*12C>T | ENSP00000489700.1:n.*12C>T | |
| ENST00000637340.1:n.3565+31C>T | ||
| ENST00000637353.1:c.1640+31C>T | ENSP00000490441.1:n.1640+31C>T | |
| ENST00000637602.1:c.*1341+31C>T | ENSP00000490074.1:n.*1341+31C>T | |
| ENST00000637849.1:n.1704+31C>T | ||
| ENST00000637892.1:n.1844+31C>T | ||
| ENST00000371068.9:c.1640+31C>T | ENSP00000360107.4:n.1640+31C>T | |
| ENST00000480623.5:c.*2060+31C>T | ENSP00000434498.1:n.*2060+31C>T | |
| ENST00000538167.2:c.1583+31C>T | ENSP00000444521.1:n.1583+31C>T | |
| NM_001172420.1:c.1583+31C>T | NP_001165891.1:n.1583+31C>T | |
| NM_018100.3:c.1640+31C>T | NP_060570.2:n.1640+31C>T | |
| NR_033327.1:n.3112+31C>T | ||
| NM_018100.4:c.1640+31C>T MANE Select | NP_060570.2:n.1640+31C>T | |
| NM_001172420.2:c.1583+31C>T | NP_001165891.1:n.1583+31C>T | |
| NR_033327.2:n.2966+31C>T |