Linked Data
MyVariant Identifiers:
chr10:g.48389336G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47350026C>G , CM000672.2:g.47350026C>G | GRCh38 |
| NC_000010.10:g.48389336G>C , CM000672.1:g.48389336G>C | GRCh37 |
| NC_000010.9:g.48009342G>C | NCBI36 |
| NG_029718.1:g.6656C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000584701.2:c.1542C>G MANE Select | ENSP00000463151.1:p.Thr514= | |
| ENST00000584701.1:c.1542C>G | ENSP00000463151.1:p.Thr514= | |
| NM_002900.2:c.1542C>G | NP_002891.1:p.Thr514= | |
| NM_002900.3:c.1542C>G MANE Select | NP_002891.1:p.Thr514= |