Linked Data
dbSNP Id:
rs1825308247
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86739669T>C , CM000670.2:g.86739669T>C | GRCh38 |
| NC_000008.10:g.87751897T>C , CM000670.1:g.87751897T>C | GRCh37 |
| NC_000008.9:g.87821013T>C | NCBI36 |
| NG_016980.1:g.9007A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.197A>G MANE Select | ENSP00000316605.5:p.His66Arg | |
| ENST00000681746.1:c.197A>G | ENSP00000505959.1:p.His66Arg | |
| ENST00000320005.5:c.197A>G | ENSP00000316605.5:p.His66Arg | |
| ENST00000519777.1:n.179A>G | ||
| NM_019098.4:c.197A>G | NP_061971.3:p.His66Arg | |
| NM_019098.5:c.197A>G MANE Select | NP_061971.3:p.His66Arg |