HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52033501C>G , CM000666.2:g.52033501C>G | GRCh38 |
NC_000004.11:g.52899667C>G , CM000666.1:g.52899667C>G | GRCh37 |
NC_000004.10:g.52594424C>G | NCBI36 |
NG_008891.1:g.9819G>C , LRG_204:g.9819G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.173G>C MANE Select | ENSP00000370839.6:p.Arg58Thr | |
ENST00000381431.9:c.173G>C | ENSP00000370839.5:p.Arg58Thr | |
ENST00000506357.5:c.159G>C | ||
ENST00000514133.1:c.140G>C | ENSP00000425818.1:p.Arg47Thr | |
NM_000232.4:c.173G>C , LRG_204t1:c.173G>C | NP_000223.1:p.Arg58Thr | |
XM_006714049.2:c.-235G>C | XP_006714112.1:n.-235G>C | |
XM_011534403.1:c.34-3638G>C | XP_011532705.1:n.34-3638G>C | |
XM_011534404.1:c.-212G>C | XP_011532706.1:n.-212G>C | |
NM_000232.5:c.173G>C MANE Select | NP_000223.1:p.Arg58Thr |