Linked Data
ClinVar Variation Id:
894759
ClinVar RCV Id:
RCV001136354
dbSNP Id:
rs943205037
gnomAD v3:
2-156329815-G-A
gnomAD v4:
2-156329815-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.156329815G>A , CM000664.2:g.156329815G>A | GRCh38 |
| NC_000002.11:g.157186327G>A , CM000664.1:g.157186327G>A | GRCh37 |
| NC_000002.10:g.156894573G>A | NCBI36 |
| NG_011821.1:g.7961C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000421709.2:c.183C>T | ENSP00000388120.2:p.Pro61= | |
| ENST00000700228.1:c.243C>T | ENSP00000514865.1:p.Pro81= | |
| ENST00000700231.1:c.372C>T | ENSP00000514868.1:p.Pro124= | |
| ENST00000339562.9:c.372C>T MANE Select | ENSP00000344479.4:p.Pro124= | |
| ENST00000675870.1:c.183C>T | ENSP00000502739.1:p.Pro61= | |
| ENST00000339562.8:c.372C>T | ENSP00000344479.4:p.Pro124= | |
| ENST00000406048.2:c.208+99C>T | ||
| ENST00000409108.6:c.372C>T | ENSP00000386993.2:p.Pro124= | |
| ENST00000409572.5:c.372C>T | ENSP00000386747.1:p.Pro124= | |
| ENST00000417764.5:c.183C>T | ENSP00000415632.1:p.Pro61= | |
| ENST00000417972.5:c.183C>T | ENSP00000394671.1:p.Pro61= | |
| ENST00000421709.1:c.183C>T | ENSP00000388120.1:p.Pro61= | |
| ENST00000424077.1:c.372C>T | ENSP00000406808.1:p.Pro124= | |
| ENST00000426264.5:c.183C>T | ENSP00000389986.1:p.Pro61= | |
| ENST00000429376.5:c.183C>T | ENSP00000410952.1:p.Pro61= | |
| NM_006186.3:c.372C>T | NP_006177.1:p.Pro124= | |
| XM_005246621.2:c.405C>T | XP_005246678.1:p.Pro135= | |
| XM_005246622.2:c.183C>T | XP_005246679.1:p.Pro61= | |
| XM_005246623.1:c.183C>T | XP_005246680.1:p.Pro61= | |
| XM_006712553.2:c.405C>T | XP_006712616.1:p.Pro135= | |
| XM_011511246.1:c.405C>T | XP_011509548.1:p.Pro135= | |
| XR_427087.2:n.2578C>T | ||
| NM_173173.2:c.183C>T | NP_775265.1:p.Pro61= | |
| XM_005246621.4:c.405C>T | XP_005246678.1:p.Pro135= | |
| XM_006712553.4:c.405C>T | XP_006712616.1:p.Pro135= | |
| XM_011511246.2:c.405C>T | XP_011509548.1:p.Pro135= | |
| XM_017004219.2:c.372C>T | XP_016859708.1:p.Pro124= | |
| XM_017004220.2:c.372C>T | XP_016859709.1:p.Pro124= | |
| XR_001738751.2:n.740C>T | ||
| XR_001738752.2:n.562C>T | ||
| XR_427087.4:n.619C>T | ||
| NM_006186.4:c.372C>T MANE Select | NP_006177.1:p.Pro124= | |
| NM_173173.3:c.183C>T | NP_775265.1:p.Pro61= |