Canonical Allele Identifier:
CA519539538
Gene:
Linked Data
MyVariant Identifiers:
chrY:g.7548863G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.7680822G>C , CM000686.2:g.7680822G>C | GRCh38 |
| NC_000024.9:g.7548863G>C , CM000686.1:g.7548863G>C | GRCh37 |
| NC_000024.8:g.7608863G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439805.1:n.574G>C |