HGVS | Genome Assembly |
---|---|
NC_000007.14:g.106659346T>C , CM000669.2:g.106659346T>C | GRCh38 |
NC_000007.13:g.106299792T>C , CM000669.1:g.106299792T>C | GRCh37 |
NC_000007.12:g.106087028T>C | NCBI36 |
NG_051955.1:g.6843A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000523505.3:c.*843A>G MANE Select | ENSP00000430897.2:n.*843A>G | |
ENST00000315965.6:c.*553A>G | ENSP00000479540.1:n.*553A>G | |
ENST00000523505.1:c.*843A>G | ENSP00000430897.1:n.*843A>G | |
NM_175884.4:c.*843A>G | NP_787080.2:n.*843A>G | |
NM_175884.5:c.*843A>G | NP_787080.2:n.*843A>G | |
XR_001745317.1:n.120-43575A>G | ||
NM_175884.6:c.*843A>G MANE Select | NP_787080.2:n.*843A>G |