HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919908G>C , CM000679.2:g.74919908G>C | GRCh38 |
NC_000017.10:g.72916003G>C , CM000679.1:g.72916003G>C | GRCh37 |
NC_000017.9:g.70427598G>C | NCBI36 |
NG_007882.1:g.8349C>G | |
NG_033062.1:g.634G>C | |
NG_007882.2:g.8356C>G | |
NG_033062.2:g.634G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614341.5:c.928C>G MANE Select | ENSP00000480279.1:p.Pro310Ala | |
ENST00000579243.1:c.*527C>G | ENSP00000462568.1:n.*527C>G | |
ENST00000614341.4:c.928C>G | ENSP00000480279.1:p.Pro310Ala | |
NM_001282489.2:c.619C>G | NP_001269418.1:p.Pro207Ala | |
NM_173477.4:c.928C>G | NP_775748.2:p.Pro310Ala | |
XM_011524296.1:c.619C>G | XP_011522598.1:p.Pro207Ala | |
XM_011524296.2:c.619C>G | XP_011522598.1:p.Pro207Ala | |
NM_173477.5:c.928C>G MANE Select | NP_775748.2:p.Pro310Ala | |
NM_001282489.3:c.619C>G | NP_001269418.1:p.Pro207Ala |