HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46240253C>T , CM000665.2:g.46240253C>T | GRCh38 |
NC_000003.11:g.46281744C>T , CM000665.1:g.46281744C>T | GRCh37 |
NC_000003.10:g.46256748C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357422.2:c.-67-2149C>T | ENSP00000350003.2:n.-67-2149C>T | |
XM_006712960.2:c.-67-2149C>T | XP_006713023.1:n.-67-2149C>T | |
XM_011533334.1:c.-154-2149C>T | XP_011531636.1:n.-154-2149C>T | |
XM_011533335.1:c.-148-2149C>T | XP_011531637.1:n.-148-2149C>T | |
XM_006712960.3:c.-67-2149C>T | XP_006713023.1:n.-67-2149C>T | |
XM_011533335.2:c.-148-2149C>T | XP_011531637.1:n.-148-2149C>T | |
XM_017005686.1:c.-965-2149C>T | XP_016861175.1:n.-965-2149C>T |