Linked Data
MyVariant Identifiers:
chrY:g.21646667A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19484781A>G , CM000686.2:g.19484781A>G | GRCh38 |
| NC_000024.9:g.21646667A>G , CM000686.1:g.21646667A>G | GRCh37 |
| NC_000024.8:g.20106055A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650676.1:n.112-4487T>C | ||
| ENST00000400605.5:n.106-4487T>C | ||
| ENST00000441139.5:n.123-4487T>C | ||
| ENST00000513194.1:n.104T>C | ||
| NR_002923.2:n.123-4487T>C | ||
| NR_033732.1:n.123-4487T>C |