Linked Data
MyVariant Identifiers:
chrY:g.17493486T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.15381606T>C , CM000686.2:g.15381606T>C | GRCh38 |
| NC_000024.9:g.17493486T>C , CM000686.1:g.17493486T>C | GRCh37 |
| NC_000024.8:g.16002880T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000421058.1:n.277A>G |