Linked Data
MyVariant Identifiers:
chrY:g.21751468G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19589582G>T , CM000686.2:g.19589582G>T | GRCh38 |
| NC_000024.9:g.21751468G>T , CM000686.1:g.21751468G>T | GRCh37 |
| NC_000024.8:g.20210856G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686158.1:n.559G>T | ||
| ENST00000686905.1:n.1644G>T | ||
| ENST00000693214.1:n.1732G>T | ||
| ENST00000445715.6:n.461G>T | ||
| ENST00000407724.7:n.805G>T | ||
| ENST00000445715.5:n.461G>T | ||
| ENST00000447202.2:n.2496G>T | ||
| ENST00000447520.5:n.461G>T | ||
| ENST00000459719.6:n.1732G>T | ||
| ENST00000538014.2:n.1751G>T | ||
| ENST00000585549.5:n.104G>T | ||
| ENST00000587095.1:n.102G>T | ||
| ENST00000588613.5:n.170G>T | ||
| ENST00000589075.5:n.143G>T | ||
| NR_045128.1:n.485G>T | ||
| NR_045129.1:n.485G>T |