Linked Data
MyVariant Identifiers:
chr10:g.135352345C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133538841C>A , CM000672.2:g.133538841C>A | GRCh38 |
| NC_000010.10:g.135352345C>A , CM000672.1:g.135352345C>A | GRCh37 |
| NC_000010.9:g.135202335C>A | NCBI36 |
| NG_008383.1:g.16479C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252945.8:c.1359C>A MANE Select | ENSP00000252945.3:p.Ala453= | |
| ENST00000252945.7:c.1359C>A | ENSP00000252945.3:p.Ala453= | |
| ENST00000368520.1:n.1358+949C>A | ||
| ENST00000463117.6:c.1359C>A | ENSP00000440689.1:p.Ala453= | |
| ENST00000469258.1:n.455C>A | ||
| NM_000773.3:c.1359C>A | NP_000764.1:p.Ala453= | |
| NM_000773.4:c.1359C>A MANE Select | NP_000764.1:p.Ala453= |