HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52488397A>G , CM000674.2:g.52488397A>G | GRCh38 |
NC_000012.11:g.52882181A>G , CM000674.1:g.52882181A>G | GRCh37 |
NC_000012.10:g.51168448A>G | NCBI36 |
NG_008298.1:g.10001T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.1355T>C MANE Select | ENSP00000369317.3:p.Met452Thr | |
ENST00000330722.6:c.1355T>C | ENSP00000369317.3:p.Met452Thr | |
NM_005554.3:c.1355T>C | NP_005545.1:p.Met452Thr | |
NM_005554.4:c.1355T>C MANE Select | NP_005545.1:p.Met452Thr |