HGVS | Genome Assembly |
---|---|
NC_000019.10:g.9126407C>A , CM000681.2:g.9126407C>A | GRCh38 |
NC_000019.9:g.9237083C>A , CM000681.1:g.9237083C>A | GRCh37 |
NC_000019.8:g.9098083C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305444.2:c.544G>T MANE Select | ENSP00000302867.2:p.Ala182Ser | |
NM_001001958.1:c.544G>T MANE Select | NP_001001958.1:p.Ala182Ser |