Linked Data
MyVariant Identifiers:
chrY:g.21751274A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19589388A>G , CM000686.2:g.19589388A>G | GRCh38 |
| NC_000024.9:g.21751274A>G , CM000686.1:g.21751274A>G | GRCh37 |
| NC_000024.8:g.20210662A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686158.1:n.498-133A>G | ||
| ENST00000686905.1:n.1450A>G | ||
| ENST00000693214.1:n.1538A>G | ||
| ENST00000445715.6:n.400-133A>G | ||
| ENST00000407724.7:n.750-139A>G | ||
| ENST00000445715.5:n.400-133A>G | ||
| ENST00000447202.2:n.2302A>G | ||
| ENST00000447520.5:n.400-133A>G | ||
| ENST00000459719.6:n.1538A>G | ||
| ENST00000538014.2:n.1557A>G | ||
| ENST00000585549.5:n.43-133A>G | ||
| ENST00000587095.1:n.41-133A>G | ||
| ENST00000588613.5:n.109-133A>G | ||
| ENST00000589075.5:n.82-133A>G | ||
| NR_045128.1:n.424-133A>G | ||
| NR_045129.1:n.424-133A>G |