HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10673807C>G , CM000682.2:g.10673807C>G | GRCh38 |
NC_000020.10:g.10654455C>G , CM000682.1:g.10654455C>G | GRCh37 |
NC_000020.9:g.10602455C>G | NCBI36 |
NG_007496.1:g.5240G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.-277G>C MANE Select | ENSP00000254958.4:n.-277G>C | |
ENST00000254958.9:c.-277G>C | ENSP00000254958.4:n.-277G>C | |
NM_000214.2:c.-277G>C | NP_000205.1:n.-277G>C | |
NM_000214.3:c.-277G>C MANE Select | NP_000205.1:n.-277G>C |