Linked Data
MyVariant Identifiers:
chrY:g.16192968T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.14081088T>G , CM000686.2:g.14081088T>G | GRCh38 |
| NC_000024.9:g.16192968T>G , CM000686.1:g.16192968T>G | GRCh37 |
| NC_000024.8:g.14702362T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000458328.1:n.14T>G |