HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919739C>A , CM000679.2:g.74919739C>A | GRCh38 |
NC_000017.10:g.72915834C>A , CM000679.1:g.72915834C>A | GRCh37 |
NC_000017.9:g.70427429C>A | NCBI36 |
NG_007882.1:g.8518G>T | |
NG_033062.1:g.465C>A | |
NG_007882.2:g.8525G>T | |
NG_033062.2:g.465C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.1097G>T MANE Select | ENSP00000480279.1:p.Arg366Leu | |
ENST00000579243.1:c.*696G>T | ENSP00000462568.1:n.*696G>T | |
ENST00000614341.4:c.1097G>T | ENSP00000480279.1:p.Arg366Leu | |
NM_001282489.2:c.788G>T | NP_001269418.1:p.Arg263Leu | |
NM_173477.4:c.1097G>T | NP_775748.2:p.Arg366Leu | |
XM_011524296.1:c.788G>T | XP_011522598.1:p.Arg263Leu | |
XM_011524296.2:c.788G>T | XP_011522598.1:p.Arg263Leu | |
NM_173477.5:c.1097G>T MANE Select | NP_775748.2:p.Arg366Leu | |
NM_001282489.3:c.788G>T | NP_001269418.1:p.Arg263Leu |