Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48974724A>T , CM000681.2:g.48974724A>T | GRCh38 |
| NC_000019.9:g.49477981A>T , CM000681.1:g.49477981A>T | GRCh37 |
| NC_000019.8:g.54169793A>T | NCBI36 |
| NG_012923.1:g.23630T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323798.8:c.1318T>A MANE Select | ENSP00000317904.3:p.Phe440Ile | |
| ENST00000263276.6:c.1126T>A | ENSP00000263276.6:p.Phe376Ile | |
| ENST00000323798.7:c.1318T>A | ENSP00000317904.3:p.Phe440Ile | |
| ENST00000472004.5:n.73T>A | ||
| ENST00000496048.1:n.225T>A | ||
| NM_001161587.1:c.1126T>A | NP_001155059.1:p.Phe376Ile | |
| NM_002103.4:c.1318T>A | NP_002094.2:p.Phe440Ile | |
| NR_027763.1:n.1377T>A | ||
| NM_002103.5:c.1318T>A MANE Select | NP_002094.2:p.Phe440Ile | |
| NM_001161587.2:c.1126T>A | NP_001155059.1:p.Phe376Ile | |
| NR_027763.2:n.1333T>A |