Linked Data
MyVariant Identifiers:
chrY:g.14498895T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12387100T>G , CM000686.2:g.12387100T>G | GRCh38 |
| NC_000024.9:g.14498895T>G , CM000686.1:g.14498895T>G | GRCh37 |
| NC_000024.8:g.13008903T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382965.3:n.317-8351A>C (GYG2P1) | ||
| ENST00000689264.1:n.402-8351A>C (GYG2P1) | ||
| ENST00000443820.2:n.1539T>G (ARSDP1) | ||
| ENST00000651802.1:n.450+19284A>C (GYG2P1) | ||
| ENST00000651835.1:n.319+19696A>C (GYG2P1) | ||
| ENST00000382966.5:n.283+19696A>C (GYG2P1) | ||
| ENST00000443820.1:n.987T>G (ARSDP1) | ||
| ENST00000493160.5:n.803-3770A>C (GYG2P1) | ||
| XR_001756061.1:n.609-8351A>C |