Linked Data
MyVariant Identifiers:
chrY:g.14077968G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.11957262G>T , CM000686.2:g.11957262G>T | GRCh38 |
| NC_000024.9:g.14077968G>T , CM000686.1:g.14077968G>T | GRCh37 |
| NC_000024.8:g.12587968G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420610.1:n.55G>T |