Linked Data
ClinVar Variation Id:
2664260
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94056722A>G , CM000663.2:g.94056722A>G | GRCh38 |
| NC_000001.10:g.94522278A>G , CM000663.1:g.94522278A>G | GRCh37 |
| NC_000001.9:g.94294866A>G | NCBI36 |
| NG_009073.1:g.69428T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.2261T>C MANE Select | ENSP00000359245.3:p.Phe754Ser | |
| ENST00000649773.1:c.2161-1407T>C | ENSP00000496882.1:n.2161-1407T>C | |
| ENST00000370225.3:c.2261T>C | ENSP00000359245.3:p.Phe754Ser | |
| ENST00000536513.5:c.-65+6452T>C | ENSP00000439707.2:n.-65+6452T>C | |
| NM_000350.2:c.2261T>C | NP_000341.2:p.Phe754Ser | |
| NM_000350.3:c.2261T>C MANE Select | NP_000341.2:p.Phe754Ser |