Linked Data
ClinVar Variation Id:
425325
dbSNP Id:
rs1064797305
gnomAD v2:
4-6303032-C-A
gnomAD v3:
4-6301305-C-A
gnomAD v4:
4-6301305-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6301305C>A , CM000666.2:g.6301305C>A | GRCh38 |
| NC_000004.11:g.6303032C>A , CM000666.1:g.6303032C>A | GRCh37 |
| NC_000004.10:g.6353933C>A | NCBI36 |
| NG_011700.1:g.36456C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.1546C>A | ENSP00000507852.1:p.Pro516Thr | |
| ENST00000683395.1:c.1487C>A | ||
| ENST00000684087.1:c.1510C>A | ENSP00000506978.1:p.Pro504Thr | |
| ENST00000506362.2:c.1261C>A | ENSP00000424103.2:p.Pro421Thr | |
| ENST00000673642.1:c.1169C>A | ENSP00000501242.1:p.Pro390His | |
| ENST00000673991.1:c.1546C>A | ENSP00000501033.1:p.Pro516Thr | |
| ENST00000226760.5:c.1510C>A MANE Select | ENSP00000226760.1:p.Pro504Thr | |
| ENST00000503569.5:c.1510C>A | ENSP00000423337.1:p.Pro504Thr | |
| ENST00000507765.1:n.1695C>A | ||
| NM_001145853.1:c.1510C>A | NP_001139325.1:p.Pro504Thr | |
| NM_006005.3:c.1510C>A MANE Select | NP_005996.2:p.Pro504Thr | |
| XM_017008586.1:c.1519C>A | XP_016864075.1:p.Pro507Thr |