HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47744750T>C , CM000679.2:g.47744750T>C | GRCh38 |
NC_000017.10:g.45822116T>C , CM000679.1:g.45822116T>C | GRCh37 |
NC_000017.9:g.43177115T>C | NCBI36 |
NG_012166.1:g.16507T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000177694.2:c.992T>C MANE Select | ENSP00000177694.1:p.Met331Thr | |
ENST00000177694.1:c.992T>C | ENSP00000177694.1:p.Met331Thr | |
NM_013351.1:c.992T>C | NP_037483.1:p.Met331Thr | |
XM_011524698.1:c.1055T>C | XP_011523000.1:p.Met352Thr | |
XM_011524699.1:c.659T>C | XP_011523001.1:p.Met220Thr | |
NM_013351.2:c.992T>C MANE Select | NP_037483.1:p.Met331Thr |