HGVS | Genome Assembly |
---|---|
NC_000010.11:g.47350139T>C , CM000672.2:g.47350139T>C | GRCh38 |
NC_000010.10:g.48389223A>G , CM000672.1:g.48389223A>G | GRCh37 |
NC_000010.9:g.48009229A>G | NCBI36 |
NG_029718.1:g.6769T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000584701.2:c.1655T>C MANE Select | ENSP00000463151.1:p.Phe552Ser | |
ENST00000584701.1:c.1655T>C | ENSP00000463151.1:p.Phe552Ser | |
NM_002900.2:c.1655T>C | NP_002891.1:p.Phe552Ser | |
NM_002900.3:c.1655T>C MANE Select | NP_002891.1:p.Phe552Ser |