Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564794C>G , CM000684.2:g.36564794C>G | GRCh38 |
| NC_000022.10:g.36960841C>G , CM000684.1:g.36960841C>G | GRCh37 |
| NC_000022.9:g.35290787C>G | NCBI36 |
| NG_031861.1:g.142850G>C | |
| NG_031861.2:g.143065G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.529G>C MANE Select | ENSP00000300105.6:p.Gly177Arg | |
| ENST00000300105.6:c.529G>C | ENSP00000300105.6:p.Gly177Arg | |
| NM_006078.3:c.529G>C | NP_006069.1:p.Gly177Arg | |
| NM_006078.4:c.529G>C | NP_006069.1:p.Gly177Arg | |
| XM_017028531.2:c.271G>C | XP_016884020.1:p.Gly91Arg | |
| NM_001379051.1:c.460G>C | NP_001365980.1:p.Gly154Arg | |
| NM_006078.5:c.529G>C MANE Select | NP_006069.1:p.Gly177Arg | |
| NR_166440.1:n.1895G>C |