HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12387285A>G , CM000686.2:g.12387285A>G | GRCh38 |
NC_000024.9:g.14499080A>G , CM000686.1:g.14499080A>G | GRCh37 |
NC_000024.8:g.13009088A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382965.3:n.317-8536T>C (GYG2P1) | ||
ENST00000689264.1:n.402-8536T>C (GYG2P1) | ||
ENST00000443820.2:n.1724A>G (ARSDP1) | ||
ENST00000651802.1:n.450+19099T>C (GYG2P1) | ||
ENST00000651835.1:n.319+19511T>C (GYG2P1) | ||
ENST00000382966.5:n.283+19511T>C (GYG2P1) | ||
ENST00000443820.1:n.1172A>G (ARSDP1) | ||
ENST00000493160.5:n.803-3955T>C (GYG2P1) | ||
XR_001756061.1:n.609-8536T>C |