HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110601648T>A , CM000672.2:g.110601648T>A | GRCh38 |
NC_000010.10:g.112361406T>A , CM000672.1:g.112361406T>A | GRCh37 |
NC_000010.9:g.112351396T>A | NCBI36 |
NG_012217.1:g.38958T>A , LRG_774:g.38958T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.4889T>A | ||
ENST00000685743.1:n.2364T>A | ||
ENST00000686057.1:n.1007T>A | ||
ENST00000689321.1:n.1619T>A | ||
ENST00000689986.1:n.445T>A | ||
ENST00000361804.5:c.2656T>A MANE Select | ENSP00000354720.5:p.Ser886Thr | |
ENST00000361804.4:c.2656T>A | ENSP00000354720.4:p.Ser886Thr | |
NM_005445.3:c.2656T>A , LRG_774t1:c.2656T>A | NP_005436.1:p.Ser886Thr | |
NM_005445.4:c.2656T>A MANE Select | NP_005436.1:p.Ser886Thr |