Linked Data
MyVariant Identifiers:
chrY:g.21645001C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19483115C>T , CM000686.2:g.19483115C>T | GRCh38 |
| NC_000024.9:g.21645001C>T , CM000686.1:g.21645001C>T | GRCh37 |
| NC_000024.8:g.20104389C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650676.1:n.112-2821G>A | ||
| ENST00000400605.5:n.106-2821G>A | ||
| ENST00000441139.5:n.123-2821G>A | ||
| ENST00000513194.1:n.1770G>A | ||
| NR_002923.2:n.123-2821G>A | ||
| NR_033732.1:n.123-2821G>A |