HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29072896A>G , CM000664.2:g.29072896A>G | GRCh38 |
NC_000002.11:g.29295762A>G , CM000664.1:g.29295762A>G | GRCh37 |
NC_000002.10:g.29149266A>G | NCBI36 |
NG_021427.1:g.6366T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.1366T>C MANE Select | ENSP00000332809.4:p.Cys456Arg | |
ENST00000331664.5:c.1366T>C | ENSP00000332809.4:p.Cys456Arg | |
NM_001029883.2:c.1366T>C | NP_001025054.1:p.Cys456Arg | |
XM_011532826.1:c.1366T>C | XP_011531128.1:p.Cys456Arg | |
XR_939901.1:n.185+3729A>G | ||
XR_939902.1:n.173+3741A>G | ||
NM_001029883.3:c.1366T>C MANE Select | NP_001025054.1:p.Cys456Arg |