Linked Data
MyVariant Identifiers:
chrY:g.14499009G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12387214G>A , CM000686.2:g.12387214G>A | GRCh38 |
| NC_000024.9:g.14499009G>A , CM000686.1:g.14499009G>A | GRCh37 |
| NC_000024.8:g.13009017G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382965.3:n.317-8465C>T (GYG2P1) | ||
| ENST00000689264.1:n.402-8465C>T (GYG2P1) | ||
| ENST00000443820.2:n.1653G>A (ARSDP1) | ||
| ENST00000651802.1:n.450+19170C>T (GYG2P1) | ||
| ENST00000651835.1:n.319+19582C>T (GYG2P1) | ||
| ENST00000382966.5:n.283+19582C>T (GYG2P1) | ||
| ENST00000443820.1:n.1101G>A (ARSDP1) | ||
| ENST00000493160.5:n.803-3884C>T (GYG2P1) | ||
| XR_001756061.1:n.609-8465C>T |