HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60644928C>A , CM000676.2:g.60644928C>A | GRCh38 |
NC_000014.8:g.61111646C>A , CM000676.1:g.61111646C>A | GRCh37 |
NC_000014.7:g.60181399C>A | NCBI36 |
NG_008231.1:g.9510G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645694.3:c.*1355G>T MANE Select | ENSP00000494686.1:n.*1355G>T | |
ENST00000247182.6:c.*1355G>T | ENSP00000247182.5:n.*1355G>T | |
ENST00000554986.2:c.*1355G>T | ENSP00000452700.2:n.*1355G>T | |
NM_005982.3:c.*1355G>T | NP_005973.1:n.*1355G>T | |
XM_017021602.2:c.*1629G>T | XP_016877091.1:n.*1629G>T | |
NM_005982.4:c.*1355G>T MANE Select | NP_005973.1:n.*1355G>T |