HGVS | Genome Assembly |
---|---|
NC_000015.10:g.80152813T>C , CM000677.2:g.80152813T>C | GRCh38 |
NC_000015.9:g.80445155T>C , CM000677.1:g.80445155T>C | GRCh37 |
NC_000015.8:g.78232210T>C | NCBI36 |
NG_012833.1:g.4815T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000558767.6:c.-242T>C | ENSP00000507680.1:n.-242T>C | |
ENST00000261755.9:c.-58T>C | ENSP00000261755.5:n.-58T>C | |
ENST00000407106.5:c.-122T>C | ENSP00000385080.1:n.-122T>C | |
ENST00000537726.5:n.25T>C | ||
ENST00000558022.5:c.-29-213T>C | ENSP00000453152.1:n.-29-213T>C | |
ENST00000558767.5:n.20T>C | ||
NM_001374377.1:c.-122T>C | NP_001361306.1:n.-122T>C | |
NM_001374380.1:c.-58T>C | NP_001361309.1:n.-58T>C |