Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7530325C>G , CM000681.2:g.7530325C>G | GRCh38 |
| NC_000019.9:g.7595211C>G , CM000681.1:g.7595211C>G | GRCh37 |
| NC_000019.8:g.7501211C>G | NCBI36 |
| NG_013374.1:g.1174C>G | |
| NG_015806.1:g.12716C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264079.11:c.1399C>G MANE Select | ENSP00000264079.5:p.Leu467Val | |
| ENST00000264079.10:c.1399C>G | ENSP00000264079.5:p.Leu467Val | |
| ENST00000394321.9:n.1714C>G | ||
| ENST00000594692.1:n.395C>G | ||
| ENST00000595860.5:n.582C>G | ||
| ENST00000599334.1:c.237-110C>G | ||
| NM_020533.2:c.1399C>G | NP_065394.1:p.Leu467Val | |
| NM_020533.3:c.1399C>G MANE Select | NP_065394.1:p.Leu467Val |