HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12383464G>C , CM000686.2:g.12383464G>C | GRCh38 |
NC_000024.9:g.14495267G>C , CM000686.1:g.14495267G>C | GRCh37 |
NC_000024.8:g.13005275G>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382965.3:n.317-4715C>G (GYG2P1) | ||
ENST00000689264.1:n.402-4715C>G (GYG2P1) | ||
ENST00000443820.2:n.1286+161G>C (ARSDP1) | ||
ENST00000651802.1:n.450+22920C>G (GYG2P1) | ||
ENST00000651835.1:n.319+23332C>G (GYG2P1) | ||
ENST00000382966.5:n.283+23332C>G (GYG2P1) | ||
ENST00000443820.1:n.734+161G>C (ARSDP1) | ||
ENST00000493160.5:n.803-134C>G (GYG2P1) | ||
XR_001756061.1:n.609-4715C>G |