Linked Data
MyVariant Identifiers:
chr13:g.48877753C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303617C>G , CM000675.2:g.48303617C>G | GRCh38 |
| NC_000013.10:g.48877753C>G , CM000675.1:g.48877753C>G | GRCh37 |
| NC_000013.9:g.47775754C>G | NCBI36 |
| NG_009009.1:g.4871C>G , LRG_517:g.4871C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046414.1:n.45G>C | ||
| NR_046414.2:n.86G>C |