Linked Data
dbSNP Id:
rs1285523018
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046337C>G , CM000667.2:g.136046337C>G | GRCh38 |
| NC_000005.9:g.135382026C>G , CM000667.1:g.135382026C>G | GRCh37 |
| NC_000005.8:g.135409925C>G | NCBI36 |
| NG_012646.1:g.22443C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.301C>G MANE Select | ENSP00000416330.2:p.Leu101Val | |
| ENST00000442011.6:c.301C>G | ENSP00000416330.2:p.Leu101Val | |
| ENST00000504185.5:n.458C>G | ||
| ENST00000506699.5:n.366C>G | ||
| ENST00000507018.5:c.218C>G | ||
| ENST00000515433.1:n.593C>G | ||
| NM_000358.2:c.301C>G | NP_000349.1:p.Leu101Val | |
| NM_000358.3:c.301C>G MANE Select | NP_000349.1:p.Leu101Val |