HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919968C>G , CM000679.2:g.74919968C>G | GRCh38 |
NC_000017.10:g.72916063C>G , CM000679.1:g.72916063C>G | GRCh37 |
NC_000017.9:g.70427658C>G | NCBI36 |
NG_007882.1:g.8289G>C | |
NG_033062.1:g.694C>G | |
NG_007882.2:g.8296G>C | |
NG_033062.2:g.694C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.868G>C MANE Select | ENSP00000480279.1:p.Ala290Pro | |
ENST00000579243.1:c.*467G>C | ENSP00000462568.1:n.*467G>C | |
ENST00000614341.4:c.868G>C | ENSP00000480279.1:p.Ala290Pro | |
NM_001282489.2:c.559G>C | NP_001269418.1:p.Ala187Pro | |
NM_173477.4:c.868G>C | NP_775748.2:p.Ala290Pro | |
XM_011524296.1:c.559G>C | XP_011522598.1:p.Ala187Pro | |
XM_011524296.2:c.559G>C | XP_011522598.1:p.Ala187Pro | |
NM_173477.5:c.868G>C MANE Select | NP_775748.2:p.Ala290Pro | |
NM_001282489.3:c.559G>C | NP_001269418.1:p.Ala187Pro |