HGVS | Genome Assembly |
---|---|
NC_000001.11:g.212883424T>A , CM000663.2:g.212883424T>A | GRCh38 |
NC_000001.10:g.213056766T>A , CM000663.1:g.213056766T>A | GRCh37 |
NC_000001.9:g.211123389T>A | NCBI36 |
NG_028131.1:g.30170T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366971.9:c.1078T>A MANE Select | ENSP00000355938.4:p.Leu360Met | |
ENST00000366971.8:c.1078T>A | ENSP00000355938.4:p.Leu360Met | |
ENST00000419102.1:c.474T>A | ||
ENST00000474693.1:n.303T>A | ||
ENST00000483790.1:n.16T>A | ||
NM_014053.3:c.1078T>A | NP_054772.1:p.Leu360Met | |
XM_011509446.1:c.1078T>A | XP_011507748.1:p.Leu360Met | |
XR_247024.1:n.1252T>A | ||
XR_426771.1:n.1379T>A | ||
XM_011509446.3:c.1078T>A | XP_011507748.1:p.Leu360Met | |
XR_247024.3:n.1252T>A | ||
NM_014053.4:c.1078T>A MANE Select | NP_054772.1:p.Leu360Met |