Linked Data
MyVariant Identifiers:
chr10:g.48388847C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47350515G>A , CM000672.2:g.47350515G>A | GRCh38 |
| NC_000010.10:g.48388847C>T , CM000672.1:g.48388847C>T | GRCh37 |
| NC_000010.9:g.48008853C>T | NCBI36 |
| NG_029718.1:g.7145G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000584701.2:c.2031G>A MANE Select | ENSP00000463151.1:p.Val677= | |
| ENST00000584701.1:c.2031G>A | ENSP00000463151.1:p.Val677= | |
| NM_002900.2:c.2031G>A | NP_002891.1:p.Val677= | |
| NM_002900.3:c.2031G>A MANE Select | NP_002891.1:p.Val677= |