Linked Data
MyVariant Identifiers:
chr5:g.59825279T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.60529452T>G , CM000667.2:g.60529452T>G | GRCh38 |
| NC_000005.9:g.59825279T>G , CM000667.1:g.59825279T>G | GRCh37 |
| NC_000005.8:g.59861036T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_024617.1:n.760T>G |