HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116748424A>G , CM000673.2:g.116748424A>G | GRCh38 |
NC_000011.9:g.116619140A>G , CM000673.1:g.116619140A>G | GRCh37 |
NC_000011.8:g.116124350A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260210.5:c.*58T>C MANE Select | ENSP00000260210.3:n.*58T>C | |
ENST00000260210.4:c.*58T>C | ENSP00000260210.3:n.*58T>C | |
ENST00000375445.7:c.*58T>C | ENSP00000364594.3:n.*58T>C | |
ENST00000419189.1:c.693T>C | ||
NM_001159736.1:c.*58T>C | NP_001153208.1:n.*58T>C | |
NM_032725.3:c.*58T>C | NP_116114.1:n.*58T>C | |
XM_011543035.1:c.*58T>C | XP_011541337.1:n.*58T>C | |
XM_011543035.2:c.*58T>C | XP_011541337.1:n.*58T>C | |
NM_032725.4:c.*58T>C MANE Select | NP_116114.1:n.*58T>C | |
NM_001159736.2:c.*58T>C | NP_001153208.1:n.*58T>C |