HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269117A>G , CM000668.2:g.31269117A>G | GRCh38 |
NC_000006.11:g.31236894A>G , CM000668.1:g.31236894A>G | GRCh37 |
NC_000006.10:g.31344873A>G | NCBI36 |
NG_029422.2:g.8015T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.*52T>C MANE Select | ENSP00000365402.5:n.*52T>C | |
ENST00000376228.9:c.*52T>C | ENSP00000365402.5:n.*52T>C | |
ENST00000376237.8:c.*740T>C | ENSP00000365412.4:n.*740T>C | |
ENST00000383329.7:c.*52T>C | ENSP00000372819.3:n.*52T>C | |
ENST00000466892.5:n.386T>C | ||
ENST00000470363.5:n.911T>C | ||
ENST00000487245.5:n.1512T>C | ||
NM_002117.5:c.*52T>C | NP_002108.4:n.*52T>C | |
NM_002117.6:c.*52T>C MANE Select | NP_002108.4:n.*52T>C |