HGVS | Genome Assembly |
---|---|
NC_000007.14:g.37888179T>C , CM000669.2:g.37888179T>C | GRCh38 |
NC_000007.13:g.37927781T>C , CM000669.1:g.37927781T>C | GRCh37 |
NC_000007.12:g.37894306T>C | NCBI36 |
NG_015893.1:g.44583T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000199447.9:c.1248-98T>C (NME8) MANE Select | ENSP00000199447.4:n.1248-98T>C | |
ENST00000199447.8:c.1248-98T>C (NME8) | ENSP00000199447.4:n.1248-98T>C | |
ENST00000426106.1:c.*194-98T>C (NME8) | ENSP00000408841.1:n.*194-98T>C | |
ENST00000440017.5:c.1248-98T>C (NME8) | ENSP00000397063.1:n.1248-98T>C | |
ENST00000476620.1:c.-38+30834T>C (EPDR1) | ENSP00000425858.1:n.-38+30834T>C | |
NM_016616.4:c.1248-98T>C (NME8) | NP_057700.3:n.1248-98T>C | |
NM_016616.5:c.1248-98T>C (NME8) MANE Select | NP_057700.3:n.1248-98T>C |