Linked Data
MyVariant Identifiers:
chr13:g.48877658C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303522C>G , CM000675.2:g.48303522C>G | GRCh38 |
| NC_000013.10:g.48877658C>G , CM000675.1:g.48877658C>G | GRCh37 |
| NC_000013.9:g.47775659C>G | NCBI36 |
| NG_009009.1:g.4776C>G , LRG_517:g.4776C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046414.1:n.140G>C | ||
| NR_046414.2:n.181G>C |