Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67435983G>A , CM000678.2:g.67435983G>A | GRCh38 |
| NC_000016.9:g.67469886G>A , CM000678.1:g.67469886G>A | GRCh37 |
| NC_000016.8:g.66027387G>A | NCBI36 |
| NG_016549.1:g.9851G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.505G>A MANE Select | ENSP00000316786.5:p.Gly169Ser | |
| ENST00000326152.5:c.505G>A | ENSP00000316786.5:p.Gly169Ser | |
| ENST00000566606.1:c.483G>A | ENSP00000473429.1:n.483G>A | |
| ENST00000567684.2:n.368G>A | ||
| NM_000196.3:c.505G>A | NP_000187.3:p.Gly169Ser | |
| NM_000196.4:c.505G>A MANE Select | NP_000187.3:p.Gly169Ser |