Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529653G>T , CM000681.2:g.7529653G>T | GRCh38 |
| NC_000019.9:g.7594539G>T , CM000681.1:g.7594539G>T | GRCh37 |
| NC_000019.8:g.7500539G>T | NCBI36 |
| NG_013374.1:g.502G>T | |
| NG_015806.1:g.12044G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.1300G>T MANE Select | ENSP00000264079.5:p.Val434Phe | |
| ENST00000264079.10:c.1300G>T | ENSP00000264079.5:p.Val434Phe | |
| ENST00000394321.9:n.1615G>T | ||
| ENST00000594692.1:n.296G>T | ||
| ENST00000595860.5:n.483G>T | ||
| ENST00000599334.1:c.177G>T | ||
| NM_020533.2:c.1300G>T | NP_065394.1:p.Val434Phe | |
| NM_020533.3:c.1300G>T MANE Select | NP_065394.1:p.Val434Phe |