HGVS | Genome Assembly |
---|---|
NC_000010.11:g.103086436T= , CM000672.2:g.103086436T= | GRCh38 |
NC_000010.10:g.104846193T= , CM000672.1:g.104846193T= | GRCh37 |
NC_000010.9:g.104836183T= | NCBI36 |
NG_042272.1:g.111871A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369878.9:c.*9256T= MANE Select | ENSP00000358894.3:n.*9256T= | |
ENST00000369878.8:c.*9256T= | ENSP00000358894.3:n.*9256T= | |
XR_001747118.1:n.12137T= | ||
XR_001747121.1:n.12101T= | ||
NM_017649.5:c.*9256T= MANE Select | NP_060119.3:n.*9256T= | |
NM_199076.3:c.*9256T= | NP_951058.1:n.*9256T= |