HGVS | Genome Assembly |
---|---|
NC_000012.12:g.14978076G>T , CM000674.2:g.14978076G>T | GRCh38 |
NC_000012.11:g.15131010G>T , CM000674.1:g.15131010G>T | GRCh37 |
NC_000012.10:g.15022277G>T | NCBI36 |
NG_016859.1:g.10055G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266395.3:c.64G>T MANE Select | ENSP00000266395.2:p.Gly22Cys | |
ENST00000266395.2:c.64G>T | ENSP00000266395.2:p.Gly22Cys | |
NM_006205.2:c.64G>T | NP_006196.1:p.Gly22Cys | |
XR_931376.1:n.175+11411C>A | ||
XM_017019431.2:c.64G>T | XP_016874920.1:p.Gly22Cys | |
XR_931376.2:n.389+11411C>A | ||
NM_006205.3:c.64G>T MANE Select | NP_006196.1:p.Gly22Cys |