HGVS | Genome Assembly |
---|---|
NC_000010.11:g.103086345G>A , CM000672.2:g.103086345G>A | GRCh38 |
NC_000010.10:g.104846102G>A , CM000672.1:g.104846102G>A | GRCh37 |
NC_000010.9:g.104836092G>A | NCBI36 |
NG_042272.1:g.111962C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369878.9:c.*9165G>A MANE Select | ENSP00000358894.3:n.*9165G>A | |
ENST00000369878.8:c.*9165G>A | ENSP00000358894.3:n.*9165G>A | |
XR_001747118.1:n.12046G>A | ||
XR_001747121.1:n.12010G>A | ||
NM_017649.5:c.*9165G>A MANE Select | NP_060119.3:n.*9165G>A | |
NM_199076.3:c.*9165G>A | NP_951058.1:n.*9165G>A |