Linked Data
dbSNP Id:
rs2045065728
gnomAD v3:
Y-19484856-G-A
gnomAD v4:
Y-19484856-G-A
MyVariant Identifiers:
chrY:g.21646742G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19484856G>A , CM000686.2:g.19484856G>A | GRCh38 |
| NC_000024.9:g.21646742G>A , CM000686.1:g.21646742G>A | GRCh37 |
| NC_000024.8:g.20106130G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650676.1:n.112-4562C>T | ||
| ENST00000400605.5:n.106-4562C>T | ||
| ENST00000441139.5:n.123-4562C>T | ||
| ENST00000513194.1:n.29C>T | ||
| NR_002923.2:n.123-4562C>T | ||
| NR_033732.1:n.123-4562C>T |