HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536323G>A , CM000679.2:g.42536323G>A | GRCh38 |
NC_000017.10:g.40688341G>A , CM000679.1:g.40688341G>A | GRCh37 |
NC_000017.9:g.37941867G>A | NCBI36 |
NG_011552.1:g.5391G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.51G>A MANE Select | ENSP00000225927.1:p.Gly17= | |
ENST00000225927.6:c.51G>A | ENSP00000225927.1:p.Gly17= | |
NM_000263.3:c.51G>A | NP_000254.2:p.Gly17= | |
XM_024450771.1:c.51G>A | XP_024306539.1:p.Gly17= | |
NM_000263.4:c.51G>A MANE Select | NP_000254.2:p.Gly17= |