HGVS | Genome Assembly |
---|---|
NC_000005.10:g.147830567T= , CM000667.2:g.147830567T= | GRCh38 |
NC_000005.9:g.147210130T= , CM000667.1:g.147210130T= | GRCh37 |
NC_000005.8:g.147190323T= | NCBI36 |
NG_008356.2:g.13665A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296695.10:c.56-937A= MANE Select | ENSP00000296695.5:n.56-937A= | |
ENST00000296695.9:c.56-937A= | ENSP00000296695.5:n.56-937A= | |
ENST00000510027.2:c.56-937A= | ENSP00000427376.1:n.56-937A= | |
NM_003122.4:c.56-937A= | NP_003113.2:n.56-937A= | |
NM_001354966.1:c.56-937A= | NP_001341895.1:n.56-937A= | |
NM_001354966.2:c.56-937A= | NP_001341895.1:n.56-937A= | |
NM_001379610.1:c.56-937A= MANE Select | NP_001366539.1:n.56-937A= | |
NM_003122.5:c.56-937A= | NP_003113.2:n.56-937A= |