Linked Data
MyVariant Identifiers:
chrY:g.21751547T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19589661T>C , CM000686.2:g.19589661T>C | GRCh38 |
| NC_000024.9:g.21751547T>C , CM000686.1:g.21751547T>C | GRCh37 |
| NC_000024.8:g.20210935T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686158.1:n.589+49T>C | ||
| ENST00000686905.1:n.1723T>C | ||
| ENST00000693214.1:n.1811T>C | ||
| ENST00000445715.6:n.491+49T>C | ||
| ENST00000407724.7:n.835+49T>C | ||
| ENST00000445715.5:n.491+49T>C | ||
| ENST00000447202.2:n.2575T>C | ||
| ENST00000447520.5:n.491+49T>C | ||
| ENST00000459719.6:n.1762+49T>C | ||
| ENST00000538014.2:n.1830T>C | ||
| ENST00000585549.5:n.134+49T>C | ||
| ENST00000587095.1:n.132+49T>C | ||
| ENST00000588613.5:n.200+49T>C | ||
| ENST00000589075.5:n.173+49T>C | ||
| NR_045128.1:n.515+49T>C | ||
| NR_045129.1:n.515+49T>C |