HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12384318C>T , CM000686.2:g.12384318C>T | GRCh38 |
NC_000024.9:g.14496121C>T , CM000686.1:g.14496121C>T | GRCh37 |
NC_000024.8:g.13006129C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382965.3:n.317-5569G>A (GYG2P1) | ||
ENST00000689264.1:n.402-5569G>A (GYG2P1) | ||
ENST00000443820.2:n.1296C>T (ARSDP1) | ||
ENST00000651802.1:n.450+22066G>A (GYG2P1) | ||
ENST00000651835.1:n.319+22478G>A (GYG2P1) | ||
ENST00000382966.5:n.283+22478G>A (GYG2P1) | ||
ENST00000443820.1:n.744C>T (ARSDP1) | ||
ENST00000493160.5:n.803-988G>A (GYG2P1) | ||
XR_001756061.1:n.609-5569G>A |