HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12379658C>T , CM000686.2:g.12379658C>T | GRCh38 |
NC_000024.9:g.14491461C>T , CM000686.1:g.14491461C>T | GRCh37 |
NC_000024.8:g.13001469C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382965.3:n.317-909G>A (GYG2P1) | ||
ENST00000689264.1:n.402-909G>A (GYG2P1) | ||
ENST00000443820.2:n.989+1836C>T (ARSDP1) | ||
ENST00000651802.1:n.450+26726G>A (GYG2P1) | ||
ENST00000651835.1:n.319+27138G>A (GYG2P1) | ||
ENST00000382966.5:n.284-24887G>A (GYG2P1) | ||
ENST00000443820.1:n.438-2678C>T (ARSDP1) | ||
XR_001756061.1:n.609-909G>A |