Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17339522T>C , CM000669.2:g.17339522T>C | GRCh38 |
| NC_000007.13:g.17379146T>C , CM000669.1:g.17379146T>C | GRCh37 |
| NC_000007.12:g.17345671T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242057.9:c.1697T>C MANE Select | ENSP00000242057.4:p.Phe566Ser | |
| ENST00000637807.1:c.1667T>C | ENSP00000490530.1:p.Phe556Ser | |
| ENST00000642825.1:c.1652T>C | ENSP00000495987.1:p.Phe551Ser | |
| ENST00000242057.8:c.1697T>C | ENSP00000242057.4:p.Phe566Ser | |
| ENST00000463496.1:c.1697T>C | ENSP00000436466.1:p.Phe566Ser | |
| ENST00000492120.1:n.679T>C | ||
| NM_001621.4:c.1697T>C | NP_001612.1:p.Phe566Ser | |
| NM_001621.5:c.1697T>C MANE Select | NP_001612.1:p.Phe566Ser |