HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73640904G>C , CM000664.2:g.73640904G>C | GRCh38 |
NC_000002.11:g.73868031G>C , CM000664.1:g.73868031G>C | GRCh37 |
NC_000002.10:g.73721539G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.*41C>G MANE Select | ENSP00000272425.3:n.*41C>G | |
ENST00000272425.3:c.*41C>G | ENSP00000272425.3:n.*41C>G | |
NM_003960.3:c.*41C>G | NP_003951.3:n.*41C>G | |
NM_003960.4:c.*41C>G MANE Select | NP_003951.3:n.*41C>G |