HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12379905A>C , CM000686.2:g.12379905A>C | GRCh38 |
NC_000024.9:g.14491708A>C , CM000686.1:g.14491708A>C | GRCh37 |
NC_000024.8:g.13001716A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382965.3:n.317-1156T>G (GYG2P1) | ||
ENST00000689264.1:n.402-1156T>G (GYG2P1) | ||
ENST00000443820.2:n.989+2083A>C (ARSDP1) | ||
ENST00000651802.1:n.450+26479T>G (GYG2P1) | ||
ENST00000651835.1:n.319+26891T>G (GYG2P1) | ||
ENST00000382966.5:n.284-25134T>G (GYG2P1) | ||
ENST00000443820.1:n.438-2431A>C (ARSDP1) | ||
XR_001756061.1:n.609-1156T>G |