Linked Data
MyVariant Identifiers:
chrY:g.17493476C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.15381596C>T , CM000686.2:g.15381596C>T | GRCh38 |
| NC_000024.9:g.17493476C>T , CM000686.1:g.17493476C>T | GRCh37 |
| NC_000024.8:g.16002870C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000421058.1:n.287G>A |