HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919671T>C , CM000679.2:g.74919671T>C | GRCh38 |
NC_000017.10:g.72915766T>C , CM000679.1:g.72915766T>C | GRCh37 |
NC_000017.9:g.70427361T>C | NCBI36 |
NG_007882.1:g.8586A>G | |
NG_033062.1:g.397T>C | |
NG_007882.2:g.8593A>G | |
NG_033062.2:g.397T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.1165A>G MANE Select | ENSP00000480279.1:p.Thr389Ala | |
ENST00000579243.1:c.*764A>G | ENSP00000462568.1:n.*764A>G | |
ENST00000614341.4:c.1165A>G | ENSP00000480279.1:p.Thr389Ala | |
NM_001282489.2:c.856A>G | NP_001269418.1:p.Thr286Ala | |
NM_173477.4:c.1165A>G | NP_775748.2:p.Thr389Ala | |
XM_011524296.1:c.856A>G | XP_011522598.1:p.Thr286Ala | |
XM_011524296.2:c.856A>G | XP_011522598.1:p.Thr286Ala | |
NM_173477.5:c.1165A>G MANE Select | NP_775748.2:p.Thr389Ala | |
NM_001282489.3:c.856A>G | NP_001269418.1:p.Thr286Ala |