HGVS | Genome Assembly |
---|---|
NC_000010.11:g.68231693G>A , CM000672.2:g.68231693G>A | GRCh38 |
NC_000010.10:g.69991450G>A , CM000672.1:g.69991450G>A | GRCh37 |
NC_000010.9:g.69661456G>A | NCBI36 |
NG_031934.1:g.5421C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373673.5:c.-16C>T MANE Select | ENSP00000362777.3:n.-16C>T | |
ENST00000373673.4:c.-16C>T | ENSP00000362777.3:n.-16C>T | |
NM_145178.3:c.-16C>T | NP_660161.1:n.-16C>T | |
NM_145178.4:c.-16C>T MANE Select | NP_660161.1:n.-16C>T |