Linked Data
MyVariant Identifiers:
chr5:g.59825300T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.60529473T>G , CM000667.2:g.60529473T>G | GRCh38 |
| NC_000005.9:g.59825300T>G , CM000667.1:g.59825300T>G | GRCh37 |
| NC_000005.8:g.59861057T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_024617.1:n.781T>G |