HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147571280C>A , CM000669.2:g.147571280C>A | GRCh38 |
NC_000007.13:g.147268372C>A , CM000669.1:g.147268372C>A | GRCh37 |
NC_000007.12:g.146899305C>A | NCBI36 |
NG_007092.2:g.1459920C>A | |
NG_007092.3:g.1460280C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.1897+9023C>A MANE Select | ENSP00000354778.3:n.1897+9023C>A | |
ENST00000636870.1:n.1759+9023C>A | ||
ENST00000637825.1:n.1380+9023C>A | ||
ENST00000638117.1:n.1800+9023C>A | ||
ENST00000361727.7:c.1897+9023C>A | ENSP00000354778.3:n.1897+9023C>A | |
NM_014141.5:c.1897+9023C>A | NP_054860.1:n.1897+9023C>A | |
XM_006715919.1:c.385+9023C>A | XP_006715982.1:n.385+9023C>A | |
XM_017011950.2:c.1897+9023C>A | XP_016867439.1:n.1897+9023C>A | |
NM_014141.6:c.1897+9023C>A MANE Select | NP_054860.1:n.1897+9023C>A |