Linked Data
ClinVar Variation Id:
798575
ClinVar RCV Id:
RCV001492745
dbSNP Id:
rs1210614574
gnomAD v2:
10-21185944-A-G
gnomAD v3:
10-20897015-A-G
gnomAD v4:
10-20897015-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.20897015A>G , CM000672.2:g.20897015A>G | GRCh38 |
| NC_000010.10:g.21185944A>G , CM000672.1:g.21185944A>G | GRCh37 |
| NC_000010.9:g.21225950A>G | NCBI36 |
| NG_017092.1:g.282173T>C , LRG_411:g.282173T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377122.9:c.96T>C MANE Select | ENSP00000366326.4:p.Pro32= | |
| ENST00000674540.1:n.383T>C | ||
| ENST00000675114.1:n.565+64657T>C | ||
| ENST00000675700.1:n.380+64657T>C | ||
| ENST00000675702.1:n.636+64657T>C | ||
| ENST00000675747.1:n.2458T>C | ||
| ENST00000377119.5:n.106T>C | ||
| ENST00000377122.8:c.96T>C | ENSP00000366326.4:p.Pro32= | |
| ENST00000417816.2:c.357+64657T>C | ENSP00000393896.2:n.357+64657T>C | |
| ENST00000434381.1:c.48T>C | ENSP00000396512.1:p.Pro16= | |
| NM_001173484.1:c.357+64657T>C | NP_001166955.1:n.357+64657T>C | |
| NM_006393.2:c.96T>C , LRG_411t2:c.96T>C | NP_006384.1:p.Pro32= | |
| NM_213569.2:c.357+64657T>C , LRG_411t1:c.357+64657T>C | NP_998734.1:n.357+64657T>C | |
| XM_005252342.3:c.96T>C | XP_005252399.1:p.Pro32= | |
| XM_005252343.3:c.96T>C | XP_005252400.1:p.Pro32= | |
| XM_005252344.3:c.96T>C | XP_005252401.1:p.Pro32= | |
| XM_011519290.1:c.48T>C | XP_011517592.1:p.Pro16= | |
| XM_011519291.1:c.48T>C | XP_011517593.1:p.Pro16= | |
| XR_242691.3:n.208T>C | ||
| XM_005252342.5:c.96T>C | XP_005252399.1:p.Pro32= | |
| XM_005252343.5:c.96T>C | XP_005252400.1:p.Pro32= | |
| XM_005252344.5:c.96T>C | XP_005252401.1:p.Pro32= | |
| XM_011519291.2:c.48T>C | XP_011517593.1:p.Pro16= | |
| XM_017015468.1:c.48T>C | XP_016870957.1:p.Pro16= | |
| XR_001746995.2:n.1692T>C | ||
| XR_001746996.1:n.411T>C | ||
| XR_242691.5:n.1692T>C | ||
| NM_001173484.2:c.357+64657T>C | NP_001166955.1:n.357+64657T>C | |
| NM_001377322.1:c.357+64657T>C | NP_001364251.1:n.357+64657T>C | |
| NM_001377323.1:c.309+64657T>C | NP_001364252.1:n.309+64657T>C | |
| NM_001377324.1:c.300+64657T>C | NP_001364253.1:n.300+64657T>C | |
| NM_001377325.1:c.291+64657T>C | NP_001364254.1:n.291+64657T>C | |
| NM_001377326.1:c.249+64657T>C | NP_001364255.1:n.249+64657T>C | |
| NM_001377327.1:c.249+64657T>C | NP_001364256.1:n.249+64657T>C | |
| NM_001377328.1:c.249+64657T>C | NP_001364257.1:n.249+64657T>C | |
| NM_006393.3:c.96T>C MANE Select | NP_006384.1:p.Pro32= |