Linked Data
MyVariant Identifiers:
chr15:g.98504175C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.97960945C>G , CM000677.2:g.97960945C>G | GRCh38 |
| NC_000015.9:g.98504175C>G , CM000677.1:g.98504175C>G | GRCh37 |
| NC_000015.8:g.96305179C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268042.7:c.84C>G MANE Select | ENSP00000268042.6:p.Arg28= | |
| ENST00000268042.6:c.84C>G | ENSP00000268042.6:p.Arg28= | |
| NM_183376.2:c.84C>G | NP_899232.2:p.Arg28= | |
| NM_183376.3:c.84C>G MANE Select | NP_899232.2:p.Arg28= |