HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12383439G>T , CM000686.2:g.12383439G>T | GRCh38 |
NC_000024.9:g.14495242G>T , CM000686.1:g.14495242G>T | GRCh37 |
NC_000024.8:g.13005250G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382965.3:n.317-4690C>A (GYG2P1) | ||
ENST00000689264.1:n.402-4690C>A (GYG2P1) | ||
ENST00000443820.2:n.1286+136G>T (ARSDP1) | ||
ENST00000651802.1:n.450+22945C>A (GYG2P1) | ||
ENST00000651835.1:n.319+23357C>A (GYG2P1) | ||
ENST00000382966.5:n.283+23357C>A (GYG2P1) | ||
ENST00000443820.1:n.734+136G>T (ARSDP1) | ||
ENST00000493160.5:n.803-109C>A (GYG2P1) | ||
XR_001756061.1:n.609-4690C>A |