HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56041547T= , CM000674.2:g.56041547T= | GRCh38 |
NC_000012.11:g.56435331T= , CM000674.1:g.56435331T= | GRCh37 |
NC_000012.10:g.54721598T= | NCBI36 |
NG_023201.1:g.4646T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356464.10:c.-357+151T= | ENSP00000348849.5:n.-357+151T= | |
XR_944989.1:n.166A= | ||
XR_944990.1:n.166A= | ||
XR_944989.3:n.457A= | ||
XR_944990.3:n.457A= |