HGVS | Genome Assembly |
---|---|
NC_000001.11:g.119753290A>C , CM000663.2:g.119753290A>C | GRCh38 |
NC_000001.10:g.120295913A>C , CM000663.1:g.120295913A>C | GRCh37 |
NC_000001.9:g.120097436A>C | NCBI36 |
NG_013348.1:g.20643T>G , LRG_447:g.20643T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369406.8:c.1284T>G MANE Select | ENSP00000358414.3:p.Asp428Glu | |
ENST00000369406.7:c.1284T>G | ENSP00000358414.3:p.Asp428Glu | |
ENST00000544913.2:c.1158T>G | ENSP00000439495.2:p.Asp386Glu | |
NM_001166107.1:c.1158T>G , LRG_447t2:c.1158T>G | NP_001159579.1:p.Asp386Glu | |
NM_005518.3:c.1284T>G , LRG_447t1:c.1284T>G | NP_005509.1:p.Asp428Glu | |
XM_011541313.1:c.1119T>G | XP_011539615.1:p.Asp373Glu | |
XM_011541313.2:c.1119T>G | XP_011539615.1:p.Asp373Glu | |
NM_005518.4:c.1284T>G MANE Select | NP_005509.1:p.Asp428Glu |