Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48974646A>G , CM000681.2:g.48974646A>G | GRCh38 |
| NC_000019.9:g.49477903A>G , CM000681.1:g.49477903A>G | GRCh37 |
| NC_000019.8:g.54169715A>G | NCBI36 |
| NG_012923.1:g.23708T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323798.8:c.1396T>C MANE Select | ENSP00000317904.3:p.Phe466Leu | |
| ENST00000263276.6:c.1204T>C | ENSP00000263276.6:p.Phe402Leu | |
| ENST00000323798.7:c.1396T>C | ENSP00000317904.3:p.Phe466Leu | |
| ENST00000472004.5:n.151T>C | ||
| ENST00000496048.1:n.303T>C | ||
| NM_001161587.1:c.1204T>C | NP_001155059.1:p.Phe402Leu | |
| NM_002103.4:c.1396T>C | NP_002094.2:p.Phe466Leu | |
| NR_027763.1:n.1455T>C | ||
| NM_002103.5:c.1396T>C MANE Select | NP_002094.2:p.Phe466Leu | |
| NM_001161587.2:c.1204T>C | NP_001155059.1:p.Phe402Leu | |
| NR_027763.2:n.1411T>C |