HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56041597G>A , CM000674.2:g.56041597G>A | GRCh38 |
NC_000012.11:g.56435381G>A , CM000674.1:g.56435381G>A | GRCh37 |
NC_000012.10:g.54721648G>A | NCBI36 |
NG_023201.1:g.4696G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356464.10:c.-357+201G>A | ENSP00000348849.5:n.-357+201G>A | |
XR_944989.1:n.116C>T | ||
XR_944990.1:n.116C>T | ||
XR_944989.3:n.407C>T | ||
XR_944990.3:n.407C>T |