Linked Data
ClinVar Variation Id:
1023390
ClinVar RCV Id:
RCV001323420
dbSNP Id:
rs761403199
ExAC:
17:61914928 G / A
gnomAD v2:
17-61914928-G-A
gnomAD v4:
17-63837568-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63837568G>A , CM000679.2:g.63837568G>A | GRCh38 |
| NC_000017.10:g.61914928G>A , CM000679.1:g.61914928G>A | GRCh37 |
| NC_000017.9:g.59268660G>A | NCBI36 |
| NG_053004.1:g.10424C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697953.1:n.162C>T | ||
| ENST00000698016.1:c.133C>T | ENSP00000513502.1:p.Pro45Ser | |
| ENST00000698022.1:c.91C>T | ENSP00000513504.1:p.Pro31Ser | |
| ENST00000698027.1:c.133C>T | ENSP00000513505.1:p.Pro45Ser | |
| ENST00000448276.7:c.274C>T MANE Select | ENSP00000392617.2:p.Pro92Ser | |
| ENST00000225742.13:c.49C>T | ENSP00000225742.9:p.Pro17Ser | |
| ENST00000323347.14:c.130C>T | ENSP00000318451.10:p.Pro44Ser | |
| ENST00000448276.6:c.274C>T | ENSP00000392617.2:p.Pro92Ser | |
| ENST00000577686.1:n.53-331C>T | ||
| ENST00000580054.1:c.58C>T | ENSP00000463793.1:p.Pro20Ser | |
| ENST00000584400.5:c.217-331C>T | ENSP00000464503.1:n.217-331C>T | |
| ENST00000613943.4:c.163C>T | ENSP00000483605.1:p.Pro55Ser | |
| NM_001098426.1:c.274C>T | NP_001091896.1:p.Pro92Ser | |
| XM_005257604.2:c.49C>T | XP_005257661.2:p.Pro17Ser | |
| NM_001330439.1:c.49C>T | NP_001317368.1:p.Pro17Ser | |
| NM_001330440.1:c.130C>T | NP_001317369.1:p.Pro44Ser | |
| NM_001098426.2:c.274C>T MANE Select | NP_001091896.1:p.Pro92Ser | |
| NM_001330440.2:c.130C>T | NP_001317369.1:p.Pro44Ser |