Linked Data
MyVariant Identifiers:
chr5:g.59825254T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.60529427T>C , CM000667.2:g.60529427T>C | GRCh38 |
| NC_000005.9:g.59825254T>C , CM000667.1:g.59825254T>C | GRCh37 |
| NC_000005.8:g.59861011T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_024617.1:n.735T>C |