Linked Data
MyVariant Identifiers:
chr10:g.69991195C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231438C>T , CM000672.2:g.68231438C>T | GRCh38 |
| NC_000010.10:g.69991195C>T , CM000672.1:g.69991195C>T | GRCh37 |
| NC_000010.9:g.69661201C>T | NCBI36 |
| NG_031934.1:g.5676G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373673.5:c.240G>A MANE Select | ENSP00000362777.3:p.Glu80= | |
| ENST00000373673.4:c.240G>A | ENSP00000362777.3:p.Glu80= | |
| NM_145178.3:c.240G>A | NP_660161.1:p.Glu80= | |
| NM_145178.4:c.240G>A MANE Select | NP_660161.1:p.Glu80= |