Linked Data
ClinVar Variation Id:
848705
ClinVar RCV Id:
RCV001052522
dbSNP Id:
rs1471999535
gnomAD v2:
1-216420056-A-C
gnomAD v3:
1-216246714-A-C
gnomAD v4:
1-216246714-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216246714A>C , CM000663.2:g.216246714A>C | GRCh38 |
| NC_000001.10:g.216420056A>C , CM000663.1:g.216420056A>C | GRCh37 |
| NC_000001.9:g.214486679A>C | NCBI36 |
| NG_009497.1:g.181683T>G | |
| NG_009497.2:g.181735T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.2680T>G MANE Select | ENSP00000305941.3:p.Phe894Val | |
| ENST00000674083.1:c.2680T>G | ENSP00000501296.1:p.Phe894Val | |
| ENST00000307340.7:c.2680T>G | ENSP00000305941.3:p.Phe894Val | |
| ENST00000366942.3:c.2680T>G | ENSP00000355909.3:p.Phe894Val | |
| NM_007123.5:c.2680T>G | NP_009054.5:p.Phe894Val | |
| NM_206933.2:c.2680T>G | NP_996816.2:p.Phe894Val | |
| NM_206933.3:c.2680T>G | NP_996816.2:p.Phe894Val | |
| NM_007123.6:c.2680T>G | NP_009054.6:p.Phe894Val | |
| NM_206933.4:c.2680T>G MANE Select | NP_996816.3:p.Phe894Val |