Linked Data
MyVariant Identifiers:
chrY:g.14496131T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12384328T>C , CM000686.2:g.12384328T>C | GRCh38 |
| NC_000024.9:g.14496131T>C , CM000686.1:g.14496131T>C | GRCh37 |
| NC_000024.8:g.13006139T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382965.3:n.317-5579A>G (GYG2P1) | ||
| ENST00000689264.1:n.402-5579A>G (GYG2P1) | ||
| ENST00000443820.2:n.1306T>C (ARSDP1) | ||
| ENST00000651802.1:n.450+22056A>G (GYG2P1) | ||
| ENST00000651835.1:n.319+22468A>G (GYG2P1) | ||
| ENST00000382966.5:n.283+22468A>G (GYG2P1) | ||
| ENST00000443820.1:n.754T>C (ARSDP1) | ||
| ENST00000493160.5:n.803-998A>G (GYG2P1) | ||
| XR_001756061.1:n.609-5579A>G |