HGVS | Genome Assembly |
---|---|
NC_000001.11:g.45500254T>C , CM000663.2:g.45500254T>C | GRCh38 |
NC_000001.10:g.45965926T>C , CM000663.1:g.45965926T>C | GRCh37 |
NC_000001.9:g.45738513T>C | NCBI36 |
NG_013378.1:g.5071T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401061.8:c.-79T>C | ENSP00000383840.4:n.-79T>C | |
NM_015506.2:c.-79T>C | NP_056321.2:n.-79T>C | |
NM_001330540.1:c.-301T>C | NP_001317469.1:n.-301T>C | |
XM_005270724.5:c.-79T>C | XP_005270781.1:n.-79T>C |