HGVS | Genome Assembly |
---|---|
NC_000010.11:g.70435632G>C , CM000672.2:g.70435632G>C | GRCh38 |
NC_000010.10:g.72195388G>C , CM000672.1:g.72195388G>C | GRCh37 |
NC_000010.9:g.71865394G>C | NCBI36 |
NG_012448.1:g.11078C>G | |
NG_012448.2:g.17317C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000287139.8:c.545C>G MANE Select | ENSP00000287139.3:p.Pro182Arg | |
ENST00000287139.7:c.545C>G | ENSP00000287139.3:p.Pro182Arg | |
ENST00000414871.1:c.380C>G | ENSP00000394468.1:p.Pro127Arg | |
NM_018055.4:c.545C>G | NP_060525.3:p.Pro182Arg | |
NM_001329906.1:c.146C>G | NP_001316835.1:p.Pro49Arg | |
XM_024448028.1:c.146C>G | XP_024303796.1:p.Pro49Arg | |
NM_018055.5:c.545C>G MANE Select | NP_060525.3:p.Pro182Arg | |
NM_001329906.2:c.146C>G | NP_001316835.1:p.Pro49Arg |