Linked Data
MyVariant Identifiers:
chr10:g.69991342C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231585C>T , CM000672.2:g.68231585C>T | GRCh38 |
| NC_000010.10:g.69991342C>T , CM000672.1:g.69991342C>T | GRCh37 |
| NC_000010.9:g.69661348C>T | NCBI36 |
| NG_031934.1:g.5529G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373673.5:c.93G>A MANE Select | ENSP00000362777.3:p.Gly31= | |
| ENST00000373673.4:c.93G>A | ENSP00000362777.3:p.Gly31= | |
| NM_145178.3:c.93G>A | NP_660161.1:p.Gly31= | |
| NM_145178.4:c.93G>A MANE Select | NP_660161.1:p.Gly31= |