HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110601994C>G , CM000672.2:g.110601994C>G | GRCh38 |
NC_000010.10:g.112361752C>G , CM000672.1:g.112361752C>G | GRCh37 |
NC_000010.9:g.112351742C>G | NCBI36 |
NG_012217.1:g.39304C>G , LRG_774:g.39304C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.5154C>G | ||
ENST00000685743.1:n.2629C>G | ||
ENST00000686057.1:n.1272C>G | ||
ENST00000689321.1:n.1884C>G | ||
ENST00000689986.1:n.710C>G | ||
ENST00000361804.5:c.2921C>G MANE Select | ENSP00000354720.5:p.Thr974Arg | |
ENST00000361804.4:c.2921C>G | ENSP00000354720.4:p.Thr974Arg | |
NM_005445.3:c.2921C>G , LRG_774t1:c.2921C>G | NP_005436.1:p.Thr974Arg | |
NM_005445.4:c.2921C>G MANE Select | NP_005436.1:p.Thr974Arg |