Linked Data
MyVariant Identifiers:
chr10:g.94405246G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92645489G>A , CM000672.2:g.92645489G>A | GRCh38 |
| NC_000010.10:g.94405246G>A , CM000672.1:g.94405246G>A | GRCh37 |
| NC_000010.9:g.94395226G>A | NCBI36 |
| NG_032580.1:g.57422G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.2394G>A MANE Select | ENSP00000260731.3:p.Val798= | |
| ENST00000676621.1:c.*912G>A | ENSP00000503639.1:n.*912G>A | |
| ENST00000676647.1:c.2187G>A | ENSP00000503394.1:p.Val729= | |
| ENST00000676757.1:c.2187G>A | ENSP00000504289.1:p.Val729= | |
| ENST00000677720.1:c.*368G>A | ENSP00000504840.1:n.*368G>A | |
| ENST00000260731.4:c.2394G>A | ENSP00000260731.3:p.Val798= | |
| NM_004523.3:c.2394G>A | NP_004514.2:p.Val798= | |
| NM_004523.4:c.2394G>A MANE Select | NP_004514.2:p.Val798= |