Linked Data
dbSNP Id:
rs9786706
gnomAD v3:
Y-12586994-C-T
gnomAD v4:
Y-12586994-C-T
MyVariant Identifiers:
chrY:g.12586994C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12586994C>T , CM000686.2:g.12586994C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000457658.6:n.653+40744C>T |