Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15879428C>A , CM000681.2:g.15879428C>A | GRCh38 |
| NC_000019.9:g.15990238C>A , CM000681.1:g.15990238C>A | GRCh37 |
| NC_000019.8:g.15851238C>A | NCBI36 |
| NG_007971.2:g.23647G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.1315G>T MANE Select | ENSP00000221700.3:p.Val439Phe | |
| ENST00000011989.11:c.1315G>T | ENSP00000011989.8:p.Val439Phe | |
| ENST00000221700.10:c.1315G>T | ENSP00000221700.3:p.Val439Phe | |
| ENST00000392846.7:n.1258G>T | ||
| ENST00000589654.2:c.103G>T | ||
| NM_001082.4:c.1315G>T | NP_001073.3:p.Val439Phe | |
| NM_001082.5:c.1315G>T MANE Select | NP_001073.3:p.Val439Phe |