HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157059397C>T , CM000667.2:g.157059397C>T | GRCh38 |
NC_000005.9:g.156486408C>T , CM000667.1:g.156486408C>T | GRCh37 |
NC_000005.8:g.156418986C>T | NCBI36 |
NG_017001.1:g.4563G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699093.1:c.-12-1442G>A | ENSP00000514125.1:n.-12-1442G>A | |
XM_011534511.1:c.-133-1321G>A | XP_011532813.1:n.-133-1321G>A | |
XM_011534513.1:c.-12-1442G>A | XP_011532815.1:n.-12-1442G>A | |
XM_024446020.1:c.-136-1318G>A | XP_024301788.1:n.-136-1318G>A | |
XM_024446021.1:c.-133-1321G>A | XP_024301789.1:n.-133-1321G>A | |
XM_024446023.1:c.-12-1442G>A | XP_024301791.1:n.-12-1442G>A |