Linked Data
MyVariant Identifiers:
chr10:g.48389291T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47350071A>C , CM000672.2:g.47350071A>C | GRCh38 |
| NC_000010.10:g.48389291T>G , CM000672.1:g.48389291T>G | GRCh37 |
| NC_000010.9:g.48009297T>G | NCBI36 |
| NG_029718.1:g.6701A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000584701.2:c.1587A>C MANE Select | ENSP00000463151.1:p.Pro529= | |
| ENST00000584701.1:c.1587A>C | ENSP00000463151.1:p.Pro529= | |
| NM_002900.2:c.1587A>C | NP_002891.1:p.Pro529= | |
| NM_002900.3:c.1587A>C MANE Select | NP_002891.1:p.Pro529= |