HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20425698G>C , CM000684.2:g.20425698G>C | GRCh38 |
NC_000022.10:g.20779987G>C , CM000684.1:g.20779987G>C | GRCh37 |
NC_000022.9:g.19109987G>C | NCBI36 |
NG_031868.2:g.17162C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622235.5:c.2278C>G MANE Select | ENSP00000477564.2:p.Pro760Ala | |
ENST00000615031.4:c.2291C>G | ENSP00000479389.1:p.Pro764Arg | |
ENST00000622235.4:c.2278C>G | ENSP00000477564.1:p.Pro760Ala | |
ENST00000623402.1:c.2293C>G | ENSP00000485276.1:p.Pro765Ala | |
NM_153334.6:c.2293C>G | NP_699165.3:p.Pro765Ala | |
NM_182895.4:c.2278C>G | NP_878315.2:p.Pro760Ala | |
NM_153334.7:c.2293C>G | NP_699165.3:p.Pro765Ala | |
NM_182895.5:c.2278C>G MANE Select | NP_878315.2:p.Pro760Ala |