Linked Data
dbSNP Id:
rs200861659
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12383440T>C , CM000686.2:g.12383440T>C | GRCh38 |
| NC_000024.9:g.14495243T>C , CM000686.1:g.14495243T>C | GRCh37 |
| NC_000024.8:g.13005251T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382965.3:n.317-4691A>G (GYG2P1) | ||
| ENST00000689264.1:n.402-4691A>G (GYG2P1) | ||
| ENST00000443820.2:n.1286+137T>C (ARSDP1) | ||
| ENST00000651802.1:n.450+22944A>G (GYG2P1) | ||
| ENST00000651835.1:n.319+23356A>G (GYG2P1) | ||
| ENST00000382966.5:n.283+23356A>G (GYG2P1) | ||
| ENST00000443820.1:n.734+137T>C (ARSDP1) | ||
| ENST00000493160.5:n.803-110A>G (GYG2P1) | ||
| XR_001756061.1:n.609-4691A>G |