HGVS | Genome Assembly |
---|---|
NC_000010.11:g.68231383C>A , CM000672.2:g.68231383C>A | GRCh38 |
NC_000010.10:g.69991140C>A , CM000672.1:g.69991140C>A | GRCh37 |
NC_000010.9:g.69661146C>A | NCBI36 |
NG_031934.1:g.5731G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373673.5:c.295G>T MANE Select | ENSP00000362777.3:p.Ala99Ser | |
ENST00000373673.4:c.295G>T | ENSP00000362777.3:p.Ala99Ser | |
NM_145178.3:c.295G>T | NP_660161.1:p.Ala99Ser | |
NM_145178.4:c.295G>T MANE Select | NP_660161.1:p.Ala99Ser |