HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65964437G>A , CM000674.2:g.65964437G>A | GRCh38 |
NC_000012.11:g.66358217G>A , CM000674.1:g.66358217G>A | GRCh37 |
NC_000012.10:g.64644484G>A | NCBI36 |
NG_016296.1:g.144978G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000403681.7:c.*1145G>A MANE Select | ENSP00000384026.2:n.*1145G>A | |
ENST00000403681.6:c.*1145G>A | ENSP00000384026.2:n.*1145G>A | |
NM_003483.4:c.*1145G>A | NP_003474.1:n.*1145G>A | |
NM_003483.6:c.*1145G>A MANE Select | NP_003474.1:n.*1145G>A |