Linked Data
MyVariant Identifiers:
chr13:g.48877786C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303650C>T , CM000675.2:g.48303650C>T | GRCh38 |
| NC_000013.10:g.48877786C>T , CM000675.1:g.48877786C>T | GRCh37 |
| NC_000013.9:g.47775787C>T | NCBI36 |
| NG_009009.1:g.4904C>T , LRG_517:g.4904C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046414.1:n.12G>A | ||
| NR_046414.2:n.53G>A |