HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47331857A>G , CM000673.2:g.47331857A>G | GRCh38 |
NC_000011.9:g.47353408A>G , CM000673.1:g.47353408A>G | GRCh37 |
NC_000011.8:g.47309984A>G | NCBI36 |
NG_007667.1:g.25846T>C , LRG_386:g.25846T>C | |
NG_029462.1:g.67482A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000545968.6:c.*14T>C MANE Select | ENSP00000442795.1:n.*14T>C | |
ENST00000256993.8:c.*14T>C | ENSP00000256993.5:n.*14T>C | |
ENST00000399249.6:c.*14T>C | ENSP00000382193.2:n.*14T>C | |
ENST00000545968.5:c.*14T>C | ENSP00000442795.1:n.*14T>C | |
NM_000256.3:c.*14T>C , LRG_386t1:c.*14T>C MANE Select | NP_000247.2:n.*14T>C | |
XM_011520117.1:c.*14T>C | XP_011518419.1:n.*14T>C | |
XM_011520118.1:c.*14T>C | XP_011518420.1:n.*14T>C |