HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12387293T>G , CM000686.2:g.12387293T>G | GRCh38 |
NC_000024.9:g.14499088T>G , CM000686.1:g.14499088T>G | GRCh37 |
NC_000024.8:g.13009096T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382965.3:n.317-8544A>C (GYG2P1) | ||
ENST00000689264.1:n.402-8544A>C (GYG2P1) | ||
ENST00000443820.2:n.1732T>G (ARSDP1) | ||
ENST00000651802.1:n.450+19091A>C (GYG2P1) | ||
ENST00000651835.1:n.319+19503A>C (GYG2P1) | ||
ENST00000382966.5:n.283+19503A>C (GYG2P1) | ||
ENST00000443820.1:n.1180T>G (ARSDP1) | ||
ENST00000493160.5:n.803-3963A>C (GYG2P1) | ||
XR_001756061.1:n.609-8544A>C |