HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46212257G>T , CM000665.2:g.46212257G>T | GRCh38 |
NC_000003.11:g.46253748G>T , CM000665.1:g.46253748G>T | GRCh37 |
NC_000003.10:g.46228752G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357422.2:c.-68+1350G>T | ENSP00000350003.2:n.-68+1350G>T | |
XM_006712960.2:c.-68+1350G>T | XP_006713023.1:n.-68+1350G>T | |
XM_011533334.1:c.-155+1350G>T | XP_011531636.1:n.-155+1350G>T | |
XM_011533335.1:c.-149+1350G>T | XP_011531637.1:n.-149+1350G>T | |
XM_006712960.3:c.-68+1350G>T | XP_006713023.1:n.-68+1350G>T | |
XM_011533335.2:c.-149+1350G>T | XP_011531637.1:n.-149+1350G>T | |
XM_017005686.1:c.-966+1350G>T | XP_016861175.1:n.-966+1350G>T |