HGVS | Genome Assembly |
---|---|
NC_000005.10:g.174724940C>G , CM000667.2:g.174724940C>G | GRCh38 |
NC_000005.9:g.174151943C>G , CM000667.1:g.174151943C>G | GRCh37 |
NC_000005.8:g.174084549C>G | NCBI36 |
NG_008124.1:g.5369C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239243.7:c.281C>G MANE Select | ENSP00000239243.5:p.Pro94Arg | |
ENST00000239243.6:c.281C>G | ENSP00000239243.5:p.Pro94Arg | |
ENST00000507785.2:c.281C>G | ENSP00000427425.1:p.Pro94Arg | |
NM_002449.4:c.281C>G | NP_002440.2:p.Pro94Arg | |
NM_001363626.1:c.281C>G | NP_001350555.1:p.Pro94Arg | |
NM_002449.5:c.281C>G MANE Select | NP_002440.2:p.Pro94Arg | |
NM_001363626.2:c.281C>G | NP_001350555.1:p.Pro94Arg |