HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75009085C>A , CM000676.2:g.75009085C>A | GRCh38 |
NC_000014.8:g.75475788C>A , CM000676.1:g.75475788C>A | GRCh37 |
NC_000014.7:g.74545541C>A | NCBI36 |
NG_013333.1:g.11177C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266126.10:c.953C>A MANE Select | ENSP00000266126.5:p.Pro318Gln | |
ENST00000266126.9:c.953C>A | ENSP00000266126.5:p.Pro318Gln | |
ENST00000556668.1:n.533C>A | ||
NM_014239.3:c.953C>A | NP_055054.1:p.Pro318Gln | |
NM_014239.4:c.953C>A MANE Select | NP_055054.1:p.Pro318Gln |