Linked Data
MyVariant Identifiers:
chr10:g.94405279A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92645522A>G , CM000672.2:g.92645522A>G | GRCh38 |
| NC_000010.10:g.94405279A>G , CM000672.1:g.94405279A>G | GRCh37 |
| NC_000010.9:g.94395259A>G | NCBI36 |
| NG_032580.1:g.57455A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.2427A>G MANE Select | ENSP00000260731.3:p.Glu809= | |
| ENST00000676621.1:c.*945A>G | ENSP00000503639.1:n.*945A>G | |
| ENST00000676647.1:c.2220A>G | ENSP00000503394.1:p.Glu740= | |
| ENST00000676757.1:c.2220A>G | ENSP00000504289.1:p.Glu740= | |
| ENST00000677720.1:c.*401A>G | ENSP00000504840.1:n.*401A>G | |
| ENST00000260731.4:c.2427A>G | ENSP00000260731.3:p.Glu809= | |
| NM_004523.3:c.2427A>G | NP_004514.2:p.Glu809= | |
| NM_004523.4:c.2427A>G MANE Select | NP_004514.2:p.Glu809= |