Linked Data
MyVariant Identifiers:
chr10:g.30602790T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30313861T>A , CM000672.2:g.30313861T>A | GRCh38 |
| NC_000010.10:g.30602790T>A , CM000672.1:g.30602790T>A | GRCh37 |
| NC_000010.9:g.30642796T>A | NCBI36 |
| NG_028096.1:g.40478A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263063.9:c.1497A>T MANE Select | ENSP00000263063.3:p.Val499= | |
| ENST00000263063.8:c.1497A>T | ENSP00000263063.3:p.Val499= | |
| ENST00000488290.5:n.3252A>T | ||
| NM_018109.3:c.1497A>T | NP_060579.3:p.Val499= | |
| NM_018109.4:c.1497A>T MANE Select | NP_060579.3:p.Val499= |