HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47333266C>A , CM000673.2:g.47333266C>A | GRCh38 |
NC_000011.9:g.47354817C>A , CM000673.1:g.47354817C>A | GRCh37 |
NC_000011.8:g.47311393C>A | NCBI36 |
NG_007667.1:g.24437G>T , LRG_386:g.24437G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.3258G>T MANE Select | ENSP00000442795.1:p.Trp1086Cys | |
ENST00000256993.8:c.3258G>T | ENSP00000256993.5:p.Trp1086Cys | |
ENST00000399249.6:c.3258G>T | ENSP00000382193.2:p.Trp1086Cys | |
ENST00000545968.5:c.3258G>T | ENSP00000442795.1:p.Trp1086Cys | |
NM_000256.3:c.3258G>T , LRG_386t1:c.3258G>T MANE Select | NP_000247.2:p.Trp1086Cys | |
XM_011520117.1:c.3240G>T | XP_011518419.1:p.Trp1080Cys | |
XM_011520118.1:c.3177G>T | XP_011518420.1:p.Trp1059Cys |