Linked Data
ClinVar Variation Id:
1012570
ClinVar RCV Id:
RCV001310593
dbSNP Id:
rs1791494484
MyVariant Identifiers:
chr7:g.107329510T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107689065T>G , CM000669.2:g.107689065T>G | GRCh38 |
| NC_000007.13:g.107329510T>G , CM000669.1:g.107329510T>G | GRCh37 |
| NC_000007.12:g.107116746T>G | NCBI36 |
| NG_008489.1:g.33431T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1014T>G MANE Select | ENSP00000494017.1:p.Pro338= | |
| ENST00000265715.7:c.1014T>G | ENSP00000265715.3:p.Pro338= | |
| NM_000441.1:c.1014T>G | NP_000432.1:p.Pro338= | |
| XM_005250425.1:c.1014T>G | XP_005250482.1:p.Pro338= | |
| XM_006716025.2:c.1014T>G | XP_006716088.1:p.Pro338= | |
| XM_005250425.2:c.1014T>G | XP_005250482.1:p.Pro338= | |
| XM_006716025.3:c.1014T>G | XP_006716088.1:p.Pro338= | |
| XM_017012318.1:c.1014T>G | XP_016867807.1:p.Pro338= | |
| NM_000441.2:c.1014T>G MANE Select | NP_000432.1:p.Pro338= |