HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29328396G>C , CM000664.2:g.29328396G>C | GRCh38 |
NC_000002.11:g.29551262G>C , CM000664.1:g.29551262G>C | GRCh37 |
NC_000002.10:g.29404766G>C | NCBI36 |
NG_009445.1:g.598171C>G , LRG_488:g.598171C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000389048.8:c.1368C>G MANE Select | ENSP00000373700.3:p.Asp456Glu | |
ENST00000389048.7:c.1368C>G | ENSP00000373700.3:p.Asp456Glu | |
ENST00000618119.4:c.237C>G | ENSP00000482733.1:p.Asp79Glu | |
NM_004304.4:c.1368C>G | NP_004295.2:p.Asp456Glu | |
XR_939920.1:n.704G>C | ||
XR_939921.1:n.680+5868G>C | ||
XR_001738688.2:n.2298C>G | ||
XR_939920.2:n.594G>C | ||
XR_939921.2:n.576+5868G>C | ||
NM_004304.5:c.1368C>G MANE Select | NP_004295.2:p.Asp456Glu |