Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714041A>C , CM000681.2:g.6714041A>C | GRCh38 |
| NC_000019.9:g.6714052A>C , CM000681.1:g.6714052A>C | GRCh37 |
| NC_000019.8:g.6665052A>C | NCBI36 |
| NG_009557.1:g.11611T>G , LRG_27:g.11611T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.601T>G | ENSP00000512083.1:p.Phe201Val | |
| ENST00000245907.11:c.724T>G MANE Select | ENSP00000245907.4:p.Phe242Val | |
| ENST00000245907.10:c.724T>G | ENSP00000245907.4:p.Phe242Val | |
| ENST00000595577.1:n.228T>G | ||
| NM_000064.3:c.724T>G | NP_000055.2:p.Phe242Val | |
| NM_000064.4:c.724T>G MANE Select | NP_000055.2:p.Phe242Val |