Linked Data
ClinVar Variation Id:
1656338
ClinVar RCV Id:
RCV002168939
dbSNP Id:
rs2129315838
gnomAD v4:
7-107689210-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107689210C>G , CM000669.2:g.107689210C>G | GRCh38 |
| NC_000007.13:g.107329655C>G , CM000669.1:g.107329655C>G | GRCh37 |
| NC_000007.12:g.107116891C>G | NCBI36 |
| NG_008489.1:g.33576C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1149+10C>G MANE Select | ENSP00000494017.1:n.1149+10C>G | |
| ENST00000265715.7:c.1149+10C>G | ENSP00000265715.3:n.1149+10C>G | |
| NM_000441.1:c.1149+10C>G | NP_000432.1:n.1149+10C>G | |
| XM_005250425.1:c.1149+10C>G | XP_005250482.1:n.1149+10C>G | |
| XM_006716025.2:c.1149+10C>G | XP_006716088.1:n.1149+10C>G | |
| XM_005250425.2:c.1149+10C>G | XP_005250482.1:n.1149+10C>G | |
| XM_006716025.3:c.1149+10C>G | XP_006716088.1:n.1149+10C>G | |
| XM_017012318.1:c.1149+10C>G | XP_016867807.1:n.1149+10C>G | |
| NM_000441.2:c.1149+10C>G MANE Select | NP_000432.1:n.1149+10C>G |