Linked Data
ClinVar Variation Id:
2956920
ClinVar RCV Id:
RCV003816631
dbSNP Id:
rs1210571334
gnomAD v2:
17-7592030-C-T
gnomAD v4:
17-7688712-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7688712C>T , CM000679.2:g.7688712C>T | GRCh38 |
| NC_000017.10:g.7592030C>T , CM000679.1:g.7592030C>T | GRCh37 |
| NC_000017.9:g.7532755C>T | NCBI36 |
| NG_017013.2:g.3839G>A , LRG_321:g.3839G>A | |
| NG_028245.1:g.7642C>T , LRG_375:g.7642C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698742.1:c.64C>T | ENSP00000513904.1:p.Pro22Ser | |
| ENST00000698743.1:c.64C>T | ENSP00000513905.1:p.Pro22Ser | |
| ENST00000698744.1:c.64C>T | ENSP00000513906.1:p.Pro22Ser | |
| ENST00000698745.1:c.64C>T | ENSP00000513907.1:p.Pro22Ser | |
| ENST00000698746.1:c.64C>T | ENSP00000513908.1:p.Pro22Ser | |
| ENST00000396463.7:c.64C>T MANE Select | ENSP00000379727.3:p.Pro22Ser | |
| ENST00000316024.9:c.64C>T | ENSP00000324203.5:p.Pro22Ser | |
| ENST00000396463.6:c.64C>T | ENSP00000379727.2:p.Pro22Ser | |
| ENST00000431639.6:c.64C>T | ENSP00000397219.2:p.Pro22Ser | |
| ENST00000457584.6:c.64C>T | ENSP00000411061.2:p.Pro22Ser | |
| ENST00000467699.5:n.150C>T | ||
| ENST00000498311.5:c.64C>T | ENSP00000432991.1:p.Pro22Ser | |
| ENST00000534050.5:c.64C>T | ENSP00000434999.1:p.Pro22Ser | |
| NM_001143990.1:c.64C>T | NP_001137462.1:p.Pro22Ser | |
| NM_001143991.1:c.64C>T | NP_001137463.1:p.Pro22Ser | |
| NM_001143992.1:c.64C>T | NP_001137464.1:p.Pro22Ser | |
| NM_018081.2:c.64C>T , LRG_375t1:c.64C>T | NP_060551.2:p.Pro22Ser | |
| XM_011523952.2:c.-569C>T | XP_011522254.1:n.-569C>T | |
| XM_024450824.1:c.-2012C>T | XP_024306592.1:n.-2012C>T | |
| XM_024450825.1:c.64C>T | XP_024306593.1:p.Pro22Ser | |
| XR_001752551.2:n.309C>T | ||
| NM_001143991.2:c.64C>T | NP_001137463.1:p.Pro22Ser | |
| NM_001143992.2:c.64C>T MANE Select | NP_001137464.1:p.Pro22Ser | |
| NM_001143990.2:c.64C>T | NP_001137462.1:p.Pro22Ser |