HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919691T>A , CM000679.2:g.74919691T>A | GRCh38 |
NC_000017.10:g.72915786T>A , CM000679.1:g.72915786T>A | GRCh37 |
NC_000017.9:g.70427381T>A | NCBI36 |
NG_007882.1:g.8566A>T | |
NG_033062.1:g.417T>A | |
NG_007882.2:g.8573A>T | |
NG_033062.2:g.417T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.1145A>T MANE Select | ENSP00000480279.1:p.Asp382Val | |
ENST00000579243.1:c.*744A>T | ENSP00000462568.1:n.*744A>T | |
ENST00000614341.4:c.1145A>T | ENSP00000480279.1:p.Asp382Val | |
NM_001282489.2:c.836A>T | NP_001269418.1:p.Asp279Val | |
NM_173477.4:c.1145A>T | NP_775748.2:p.Asp382Val | |
XM_011524296.1:c.836A>T | XP_011522598.1:p.Asp279Val | |
XM_011524296.2:c.836A>T | XP_011522598.1:p.Asp279Val | |
NM_173477.5:c.1145A>T MANE Select | NP_775748.2:p.Asp382Val | |
NM_001282489.3:c.836A>T | NP_001269418.1:p.Asp279Val |