HGVS | Genome Assembly |
---|---|
NC_000009.12:g.69035717T>G , CM000671.2:g.69035717T>G | GRCh38 |
NC_000009.11:g.71650633T>G , CM000671.1:g.71650633T>G | GRCh37 |
NC_000009.10:g.70840453T>G | NCBI36 |
NG_008845.2:g.5155T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377270.7:c.-66T>G | ENSP00000366482.3:n.-66T>G | |
ENST00000396364.7:c.-66T>G | ENSP00000379650.3:n.-66T>G | |
NM_000144.4:c.-66T>G | NP_000135.2:n.-66T>G | |
NM_001161706.1:c.-66T>G | NP_001155178.1:n.-66T>G | |
NM_181425.2:c.-66T>G | NP_852090.1:n.-66T>G |