Linked Data
MyVariant Identifiers:
chrY:g.21646665A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19484779A>C , CM000686.2:g.19484779A>C | GRCh38 |
| NC_000024.9:g.21646665A>C , CM000686.1:g.21646665A>C | GRCh37 |
| NC_000024.8:g.20106053A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650676.1:n.112-4485T>G | ||
| ENST00000400605.5:n.106-4485T>G | ||
| ENST00000441139.5:n.123-4485T>G | ||
| ENST00000513194.1:n.106T>G | ||
| NR_002923.2:n.123-4485T>G | ||
| NR_033732.1:n.123-4485T>G |