HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129529062G>C , CM000665.2:g.129529062G>C | GRCh38 |
NC_000003.11:g.129247905G>C , CM000665.1:g.129247905G>C | GRCh37 |
NC_000003.10:g.130730595G>C | NCBI36 |
NG_009115.1:g.5424G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.329G>C MANE Select | ENSP00000296271.3:p.Cys110Ser | |
ENST00000296271.3:c.329G>C | ENSP00000296271.3:p.Cys110Ser | |
NM_000539.3:c.329G>C MANE Select | NP_000530.1:p.Cys110Ser |