Linked Data
MyVariant Identifiers:
chrY:g.21628349C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19466463C>A , CM000686.2:g.19466463C>A | GRCh38 |
| NC_000024.9:g.21628349C>A , CM000686.1:g.21628349C>A | GRCh37 |
| NC_000024.8:g.20087737C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650676.1:n.1653G>T | ||
| ENST00000400605.5:n.1647G>T | ||
| ENST00000441139.5:n.1664G>T | ||
| ENST00000513194.1:n.4560G>T | ||
| NR_002923.2:n.1664G>T | ||
| NR_033732.1:n.1664G>T |