HGVS | Genome Assembly |
---|---|
NC_000003.12:g.114181373A>T , CM000665.2:g.114181373A>T | GRCh38 |
NC_000003.11:g.113900220A>T , CM000665.1:g.113900220A>T | GRCh37 |
NC_000003.10:g.115382910A>T | NCBI36 |
NG_008842.2:g.23035T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460779.5:c.-155-2597T>A | ENSP00000419402.1:n.-155-2597T>A | |
NM_001282563.2:c.-155-2597T>A | NP_001269492.1:n.-155-2597T>A | |
XM_011512510.1:c.-155-2597T>A | XP_011510812.1:n.-155-2597T>A | |
XM_011512511.1:c.-155-2597T>A | XP_011510813.1:n.-155-2597T>A | |
XM_011512512.1:c.-155-2597T>A | XP_011510814.1:n.-155-2597T>A | |
XM_017005829.1:c.-155-2597T>A | XP_016861318.1:n.-155-2597T>A |