HGVS | Genome Assembly |
---|---|
NC_000010.11:g.68231690G>C , CM000672.2:g.68231690G>C | GRCh38 |
NC_000010.10:g.69991447G>C , CM000672.1:g.69991447G>C | GRCh37 |
NC_000010.9:g.69661453G>C | NCBI36 |
NG_031934.1:g.5424C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373673.5:c.-13C>G MANE Select | ENSP00000362777.3:n.-13C>G | |
ENST00000373673.4:c.-13C>G | ENSP00000362777.3:n.-13C>G | |
NM_145178.3:c.-13C>G | NP_660161.1:n.-13C>G | |
NM_145178.4:c.-13C>G MANE Select | NP_660161.1:n.-13C>G |