Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7528927T>G , CM000681.2:g.7528927T>G | GRCh38 |
| NC_000019.9:g.7593813T>G , CM000681.1:g.7593813T>G | GRCh37 |
| NC_000019.8:g.7499813T>G | NCBI36 |
| NG_015806.1:g.11318T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264079.11:c.1091T>G MANE Select | ENSP00000264079.5:p.Leu364Arg | |
| ENST00000264079.10:c.1091T>G | ENSP00000264079.5:p.Leu364Arg | |
| ENST00000394321.9:n.1406T>G | ||
| ENST00000595860.5:n.274T>G | ||
| NM_020533.2:c.1091T>G | NP_065394.1:p.Leu364Arg | |
| NM_020533.3:c.1091T>G MANE Select | NP_065394.1:p.Leu364Arg |