HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69648040C>A , CM000673.2:g.69648040C>A | GRCh38 |
NC_000011.9:g.69462808C>A , CM000673.1:g.69462808C>A | GRCh37 |
NC_000011.8:g.69171989C>A | NCBI36 |
NG_007375.1:g.11936C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227507.3:c.621C>A MANE Select | ENSP00000227507.2:p.Ser207Arg | |
ENST00000227507.2:c.621C>A | ENSP00000227507.2:p.Ser207Arg | |
ENST00000536559.1:c.*41C>A | ENSP00000438482.1:n.*41C>A | |
ENST00000542367.1:n.84C>A | ||
ENST00000545484.1:n.327C>A | ||
NM_053056.2:c.621C>A | NP_444284.1:p.Ser207Arg | |
XM_006718653.2:c.645C>A | XP_006718716.1:p.Ser215Arg | |
NM_053056.3:c.621C>A MANE Select | NP_444284.1:p.Ser207Arg |