HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20425682T>G , CM000684.2:g.20425682T>G | GRCh38 |
NC_000022.10:g.20779972T>G , CM000684.1:g.20779972T>G | GRCh37 |
NC_000022.9:g.19109972T>G | NCBI36 |
NG_031868.2:g.17178A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622235.5:c.2294A>C MANE Select | ENSP00000477564.2:p.Glu765Ala | |
ENST00000615031.4:c.2306A>C | ENSP00000479389.1:p.Glu769Ala | |
ENST00000622235.4:c.2294A>C | ENSP00000477564.1:p.Glu765Ala | |
ENST00000623402.1:c.2309A>C | ENSP00000485276.1:p.Glu770Ala | |
NM_153334.6:c.2309A>C | NP_699165.3:p.Glu770Ala | |
NM_182895.4:c.2294A>C | NP_878315.2:p.Glu765Ala | |
NM_153334.7:c.2309A>C | NP_699165.3:p.Glu770Ala | |
NM_182895.5:c.2294A>C MANE Select | NP_878315.2:p.Glu765Ala |