Linked Data
MyVariant Identifiers:
chrY:g.21751545T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19589659T>G , CM000686.2:g.19589659T>G | GRCh38 |
| NC_000024.9:g.21751545T>G , CM000686.1:g.21751545T>G | GRCh37 |
| NC_000024.8:g.20210933T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686158.1:n.589+47T>G | ||
| ENST00000686905.1:n.1721T>G | ||
| ENST00000693214.1:n.1809T>G | ||
| ENST00000445715.6:n.491+47T>G | ||
| ENST00000407724.7:n.835+47T>G | ||
| ENST00000445715.5:n.491+47T>G | ||
| ENST00000447202.2:n.2573T>G | ||
| ENST00000447520.5:n.491+47T>G | ||
| ENST00000459719.6:n.1762+47T>G | ||
| ENST00000538014.2:n.1828T>G | ||
| ENST00000585549.5:n.134+47T>G | ||
| ENST00000587095.1:n.132+47T>G | ||
| ENST00000588613.5:n.200+47T>G | ||
| ENST00000589075.5:n.173+47T>G | ||
| NR_045128.1:n.515+47T>G | ||
| NR_045129.1:n.515+47T>G |