HGVS | Genome Assembly |
---|---|
NC_000010.11:g.103086416T>A , CM000672.2:g.103086416T>A | GRCh38 |
NC_000010.10:g.104846173T>A , CM000672.1:g.104846173T>A | GRCh37 |
NC_000010.9:g.104836163T>A | NCBI36 |
NG_042272.1:g.111891A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369878.9:c.*9236T>A MANE Select | ENSP00000358894.3:n.*9236T>A | |
ENST00000369878.8:c.*9236T>A | ENSP00000358894.3:n.*9236T>A | |
XR_001747118.1:n.12117T>A | ||
XR_001747121.1:n.12081T>A | ||
NM_017649.5:c.*9236T>A MANE Select | NP_060119.3:n.*9236T>A | |
NM_199076.3:c.*9236T>A | NP_951058.1:n.*9236T>A |