Linked Data
ClinVar Variation Id:
334701
dbSNP Id:
rs886055724
gnomAD v2:
2-227872818-C-T
gnomAD v3:
2-227008102-C-T
gnomAD v4:
2-227008102-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.227008102C>T , CM000664.2:g.227008102C>T | GRCh38 |
| NC_000002.11:g.227872818C>T , CM000664.1:g.227872818C>T | GRCh37 |
| NC_000002.10:g.227581062C>T | NCBI36 |
| NG_011592.1:g.161458G>A , LRG_231:g.161458G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682098.1:c.327G>A | ENSP00000508331.1:p.Ala109= | |
| ENST00000396625.5:c.4725G>A MANE Select | ENSP00000379866.3:p.Ala1575= | |
| ENST00000396625.3:c.4725G>A | ENSP00000379866.3:p.Ala1575= | |
| NM_000092.4:c.4725G>A , LRG_231t1:c.4725G>A | NP_000083.3:p.Ala1575= | |
| XM_005246281.2:c.4725G>A | XP_005246338.1:p.Ala1575= | |
| XM_005246282.2:c.4170G>A | XP_005246339.1:p.Ala1390= | |
| XM_006712246.2:c.4536G>A | XP_006712309.1:p.Ala1512= | |
| XM_006712249.2:c.4725G>A | XP_006712312.1:p.Ala1575= | |
| XM_006712252.2:c.4216+13946G>A | XP_006712315.1:n.4216+13946G>A | |
| XM_011510557.1:c.4644G>A | XP_011508859.1:p.Ala1548= | |
| XM_011510558.1:c.4617G>A | XP_011508860.1:p.Ala1539= | |
| XM_011510559.1:c.4725G>A | XP_011508861.1:p.Ala1575= | |
| XM_011510560.1:c.4725G>A | XP_011508862.1:p.Ala1575= | |
| XM_011510561.1:c.4725G>A | XP_011508863.1:p.Ala1575= | |
| XM_011510562.1:c.4725G>A | XP_011508864.1:p.Ala1575= | |
| XM_011510563.1:c.*58G>A | XP_011508865.1:n.*58G>A | |
| XM_011510564.1:c.*58G>A | XP_011508866.1:n.*58G>A | |
| XM_011510565.1:c.4216+13946G>A | XP_011508867.1:n.4216+13946G>A | |
| XM_011510566.1:c.4216+13946G>A | XP_011508868.1:n.4216+13946G>A | |
| XM_011510567.1:c.4216+13946G>A | XP_011508869.1:n.4216+13946G>A | |
| XM_011510569.1:c.4216+13946G>A | XP_011508871.1:n.4216+13946G>A | |
| XM_011510570.1:c.4216+13946G>A | XP_011508872.1:n.4216+13946G>A | |
| XM_011510571.1:c.4216+13946G>A | XP_011508873.1:n.4216+13946G>A | |
| XM_011510572.1:c.3051G>A | XP_011508874.1:p.Ala1017= | |
| XR_922837.1:n.5035G>A | ||
| XR_922838.1:n.5035G>A | ||
| XR_922839.1:n.4526+13946G>A | ||
| XR_922840.1:n.4526+13946G>A | ||
| XM_005246281.3:c.4725G>A | XP_005246338.1:p.Ala1575= | |
| XM_005246282.3:c.4170G>A | XP_005246339.1:p.Ala1390= | |
| XM_006712246.3:c.4536G>A | XP_006712309.1:p.Ala1512= | |
| XM_011510557.2:c.4644G>A | XP_011508859.1:p.Ala1548= | |
| XM_011510558.2:c.4617G>A | XP_011508860.1:p.Ala1539= | |
| XM_011510559.2:c.4725G>A | XP_011508861.1:p.Ala1575= | |
| XM_011510560.2:c.4725G>A | XP_011508862.1:p.Ala1575= | |
| XM_011510561.2:c.4725G>A | XP_011508863.1:p.Ala1575= | |
| XM_011510562.2:c.4725G>A | XP_011508864.1:p.Ala1575= | |
| XM_011510565.2:c.4216+13946G>A | XP_011508867.1:n.4216+13946G>A | |
| XM_011510566.2:c.4216+13946G>A | XP_011508868.1:n.4216+13946G>A | |
| XM_011510567.2:c.4216+13946G>A | XP_011508869.1:n.4216+13946G>A | |
| XM_011510569.2:c.4216+13946G>A | XP_011508871.1:n.4216+13946G>A | |
| XM_011510570.2:c.4216+13946G>A | XP_011508872.1:n.4216+13946G>A | |
| XM_011510572.3:c.3051G>A | XP_011508874.1:p.Ala1017= | |
| XM_017003296.1:c.4725G>A | XP_016858785.1:p.Ala1575= | |
| XM_017003297.1:c.4608G>A | XP_016858786.1:p.Ala1536= | |
| XM_017003298.1:c.4725G>A | XP_016858787.1:p.Ala1575= | |
| XM_017003300.1:c.4216+13946G>A | XP_016858789.1:n.4216+13946G>A | |
| XR_001738602.1:n.5051G>A | ||
| XR_001738603.1:n.5051G>A | ||
| XR_001738604.1:n.4797G>A | ||
| XR_001738606.1:n.4542+13946G>A | ||
| XR_001738607.1:n.4542+13946G>A | ||
| XR_922837.2:n.5051G>A | ||
| NM_000092.5:c.4725G>A MANE Select | NP_000083.3:p.Ala1575= |