HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116748439T>C , CM000673.2:g.116748439T>C | GRCh38 |
NC_000011.9:g.116619155T>C , CM000673.1:g.116619155T>C | GRCh37 |
NC_000011.8:g.116124365T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260210.5:c.*43A>G MANE Select | ENSP00000260210.3:n.*43A>G | |
ENST00000260210.4:c.*43A>G | ENSP00000260210.3:n.*43A>G | |
ENST00000375445.7:c.*43A>G | ENSP00000364594.3:n.*43A>G | |
ENST00000419189.1:c.678A>G | ||
NM_001159736.1:c.*43A>G | NP_001153208.1:n.*43A>G | |
NM_032725.3:c.*43A>G | NP_116114.1:n.*43A>G | |
XM_011543035.1:c.*43A>G | XP_011541337.1:n.*43A>G | |
XM_011543035.2:c.*43A>G | XP_011541337.1:n.*43A>G | |
NM_032725.4:c.*43A>G MANE Select | NP_116114.1:n.*43A>G | |
NM_001159736.2:c.*43A>G | NP_001153208.1:n.*43A>G |