Linked Data
MyVariant Identifiers:
chrY:g.21751492T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19589606T>G , CM000686.2:g.19589606T>G | GRCh38 |
| NC_000024.9:g.21751492T>G , CM000686.1:g.21751492T>G | GRCh37 |
| NC_000024.8:g.20210880T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686158.1:n.583T>G | ||
| ENST00000686905.1:n.1668T>G | ||
| ENST00000693214.1:n.1756T>G | ||
| ENST00000445715.6:n.485T>G | ||
| ENST00000407724.7:n.829T>G | ||
| ENST00000445715.5:n.485T>G | ||
| ENST00000447202.2:n.2520T>G | ||
| ENST00000447520.5:n.485T>G | ||
| ENST00000459719.6:n.1756T>G | ||
| ENST00000538014.2:n.1775T>G | ||
| ENST00000585549.5:n.128T>G | ||
| ENST00000587095.1:n.126T>G | ||
| ENST00000588613.5:n.194T>G | ||
| ENST00000589075.5:n.167T>G | ||
| NR_045128.1:n.509T>G | ||
| NR_045129.1:n.509T>G |