Canonical Allele Identifier:
CA519539644
Gene:
Linked Data
MyVariant Identifiers:
chrY:g.7548872C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.7680831C>A , CM000686.2:g.7680831C>A | GRCh38 |
| NC_000024.9:g.7548872C>A , CM000686.1:g.7548872C>A | GRCh37 |
| NC_000024.8:g.7608872C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439805.1:n.583C>A |