Linked Data
MyVariant Identifiers:
chrY:g.14077981T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.11957275T>A , CM000686.2:g.11957275T>A | GRCh38 |
| NC_000024.9:g.14077981T>A , CM000686.1:g.14077981T>A | GRCh37 |
| NC_000024.8:g.12587981T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420610.1:n.68T>A |