HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6780819T>C , CM000679.2:g.6780819T>C | GRCh38 |
NC_000017.10:g.6684138T>C , CM000679.1:g.6684138T>C | GRCh37 |
NC_000017.9:g.6624862T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321535.5:c.951T>C MANE Select | ENSP00000321386.4:p.Tyr317= | |
ENST00000321535.4:c.951T>C | ENSP00000321386.4:p.Tyr317= | |
NM_153230.2:c.951T>C | NP_694962.1:p.Tyr317= | |
XM_011523697.1:c.951T>C | XP_011521999.1:p.Tyr317= | |
XR_243544.3:n.1129T>C | ||
NM_153230.3:c.951T>C MANE Select | NP_694962.1:p.Tyr317= |