Linked Data
MyVariant Identifiers:
chr16:g.52586162G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.52552250G>T , CM000678.2:g.52552250G>T | GRCh38 |
| NC_000016.9:g.52586162G>T , CM000678.1:g.52586162G>T | GRCh37 |
| NC_000016.8:g.51143663G>T | NCBI36 |
| NG_012623.1:g.553C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_033920.1:n.838C>A |