Linked Data
MyVariant Identifiers:
chrY:g.21751299T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19589413T>A , CM000686.2:g.19589413T>A | GRCh38 |
| NC_000024.9:g.21751299T>A , CM000686.1:g.21751299T>A | GRCh37 |
| NC_000024.8:g.20210687T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686158.1:n.498-108T>A | ||
| ENST00000686905.1:n.1475T>A | ||
| ENST00000693214.1:n.1563T>A | ||
| ENST00000445715.6:n.400-108T>A | ||
| ENST00000407724.7:n.750-114T>A | ||
| ENST00000445715.5:n.400-108T>A | ||
| ENST00000447202.2:n.2327T>A | ||
| ENST00000447520.5:n.400-108T>A | ||
| ENST00000459719.6:n.1563T>A | ||
| ENST00000538014.2:n.1582T>A | ||
| ENST00000585549.5:n.43-108T>A | ||
| ENST00000587095.1:n.41-108T>A | ||
| ENST00000588613.5:n.109-108T>A | ||
| ENST00000589075.5:n.82-108T>A | ||
| NR_045128.1:n.424-108T>A | ||
| NR_045129.1:n.424-108T>A |