Linked Data
MyVariant Identifiers:
chr5:g.59825309A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.60529482A>T , CM000667.2:g.60529482A>T | GRCh38 |
| NC_000005.9:g.59825309A>T , CM000667.1:g.59825309A>T | GRCh37 |
| NC_000005.8:g.59861066A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_024617.1:n.790A>T |