Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583577T>A , CM000679.2:g.41583577T>A | GRCh38 |
| NC_000017.10:g.39739829T>A , CM000679.1:g.39739829T>A | GRCh37 |
| NC_000017.9:g.36993355T>A | NCBI36 |
| NG_008624.1:g.8319A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.1027A>T MANE Select | ENSP00000167586.6:p.Ile343Phe | |
| ENST00000167586.6:c.1027A>T | ENSP00000167586.6:p.Ile343Phe | |
| ENST00000476662.1:n.477A>T | ||
| NM_000526.4:c.1027A>T | NP_000517.2:p.Ile343Phe | |
| NM_000526.5:c.1027A>T MANE Select | NP_000517.3:p.Ile343Phe |