HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12718111C>G , CM000674.2:g.12718111C>G | GRCh38 |
NC_000012.11:g.12871045C>G , CM000674.1:g.12871045C>G | GRCh37 |
NC_000012.10:g.12762312C>G | NCBI36 |
NG_016341.1:g.5744C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614874.2:c.272C>G | ENSP00000507272.1:p.Pro91Arg | |
ENST00000682620.1:n.1631-714C>G | ||
ENST00000684771.1:n.585-714C>G | ||
ENST00000228872.9:c.272C>G MANE Select | ENSP00000228872.4:p.Pro91Arg | |
ENST00000228872.8:c.272C>G | ENSP00000228872.4:p.Pro91Arg | |
ENST00000396340.1:c.272C>G | ENSP00000379629.1:p.Pro91Arg | |
ENST00000442489.1:c.193+58C>G | ENSP00000407597.1:n.193+58C>G | |
ENST00000477087.1:n.155-714C>G | ||
NM_004064.4:c.272C>G | NP_004055.1:p.Pro91Arg | |
NM_004064.5:c.272C>G MANE Select | NP_004055.1:p.Pro91Arg |