HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12379814T>C , CM000686.2:g.12379814T>C | GRCh38 |
NC_000024.9:g.14491617T>C , CM000686.1:g.14491617T>C | GRCh37 |
NC_000024.8:g.13001625T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382965.3:n.317-1065A>G (GYG2P1) | ||
ENST00000689264.1:n.402-1065A>G (GYG2P1) | ||
ENST00000443820.2:n.989+1992T>C (ARSDP1) | ||
ENST00000651802.1:n.450+26570A>G (GYG2P1) | ||
ENST00000651835.1:n.319+26982A>G (GYG2P1) | ||
ENST00000382966.5:n.284-25043A>G (GYG2P1) | ||
ENST00000443820.1:n.438-2522T>C (ARSDP1) | ||
XR_001756061.1:n.609-1065A>G |