HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74755046C>A , CM000677.2:g.74755046C>A | GRCh38 |
NC_000015.9:g.75047387C>A , CM000677.1:g.75047387C>A | GRCh37 |
NC_000015.8:g.72834440C>A | NCBI36 |
NG_008431.1:g.37505C>A | |
NG_008431.2:g.37505C>A | |
NG_061543.1:g.11202C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343932.5:c.1509C>A MANE Select | ENSP00000342007.4:p.Arg503= | |
ENST00000343932.4:c.1509C>A | ENSP00000342007.4:p.Arg503= | |
NM_000761.4:c.1509C>A | NP_000752.2:p.Arg503= | |
NM_000761.5:c.1509C>A MANE Select | NP_000752.2:p.Arg503= |