HGVS | Genome Assembly |
---|---|
NC_000017.11:g.72124020A>C , CM000679.2:g.72124020A>C | GRCh38 |
NC_000017.10:g.70120161A>C , CM000679.1:g.70120161A>C | GRCh37 |
NC_000017.9:g.67631756A>C | NCBI36 |
NG_012490.1:g.8001A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000245479.3:c.1163A>C MANE Select | ENSP00000245479.2:p.Glu388Ala | |
ENST00000245479.2:c.1163A>C | ENSP00000245479.2:p.Glu388Ala | |
NM_000346.3:c.1163A>C | NP_000337.1:p.Glu388Ala | |
NM_000346.4:c.1163A>C MANE Select | NP_000337.1:p.Glu388Ala |