Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186199063C>G , CM000666.2:g.186199063C>G | GRCh38 |
| NC_000004.11:g.187120217C>G , CM000666.1:g.187120217C>G | GRCh37 |
| NC_000004.10:g.187357211C>G | NCBI36 |
| NG_007965.1:g.12544C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.781C>G MANE Select | ENSP00000368079.4:p.Leu261Val | |
| ENST00000378802.4:c.781C>G | ENSP00000368079.4:p.Leu261Val | |
| ENST00000507209.5:n.1622C>G | ||
| NM_207352.3:c.781C>G | NP_997235.3:p.Leu261Val | |
| XM_005262935.2:c.781C>G | XP_005262992.1:p.Leu261Val | |
| XM_006714184.2:c.385C>G | XP_006714247.1:p.Leu129Val | |
| XM_005262935.4:c.781C>G | XP_005262992.1:p.Leu261Val | |
| XM_017008037.1:c.385C>G | XP_016863526.1:p.Leu129Val | |
| NM_207352.4:c.781C>G MANE Select | NP_997235.3:p.Leu261Val |