Linked Data
MyVariant Identifiers:
chr15:g.45543990G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45251792G>C , CM000677.2:g.45251792G>C | GRCh38 |
| NC_000015.9:g.45543990G>C , CM000677.1:g.45543990G>C | GRCh37 |
| NC_000015.8:g.43331282G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120335.1:n.461C>G |