HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110601994C>A , CM000672.2:g.110601994C>A | GRCh38 |
NC_000010.10:g.112361752C>A , CM000672.1:g.112361752C>A | GRCh37 |
NC_000010.9:g.112351742C>A | NCBI36 |
NG_012217.1:g.39304C>A , LRG_774:g.39304C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.5154C>A | ||
ENST00000685743.1:n.2629C>A | ||
ENST00000686057.1:n.1272C>A | ||
ENST00000689321.1:n.1884C>A | ||
ENST00000689986.1:n.710C>A | ||
ENST00000361804.5:c.2921C>A MANE Select | ENSP00000354720.5:p.Thr974Lys | |
ENST00000361804.4:c.2921C>A | ENSP00000354720.4:p.Thr974Lys | |
NM_005445.3:c.2921C>A , LRG_774t1:c.2921C>A | NP_005436.1:p.Thr974Lys | |
NM_005445.4:c.2921C>A MANE Select | NP_005436.1:p.Thr974Lys |