HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47283470C>G , CM000679.2:g.47283470C>G | GRCh38 |
NC_000017.10:g.45360836C>G , CM000679.1:g.45360836C>G | GRCh37 |
NC_000017.9:g.42715835C>G | NCBI36 |
NG_008332.2:g.34629C>G , LRG_481:g.34629C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.282C>G | ENSP00000513002.1:p.Pro94= | |
ENST00000559488.7:c.282C>G MANE Select | ENSP00000452786.2:p.Pro94= | |
ENST00000559488.5:c.282C>G | ENSP00000452786.1:p.Pro94= | |
ENST00000560629.1:c.247C>G | ||
ENST00000571680.1:c.282C>G | ENSP00000461626.1:p.Pro94= | |
NM_000212.2:c.282C>G , LRG_481t1:c.282C>G | NP_000203.2:p.Pro94= | |
NM_000212.3:c.282C>G MANE Select | NP_000203.2:p.Pro94= |