HGVS | Genome Assembly |
---|---|
NC_000003.12:g.10698992T>G , CM000665.2:g.10698992T>G | GRCh38 |
NC_000003.11:g.10740677T>G , CM000665.1:g.10740677T>G | GRCh37 |
NC_000003.10:g.10715677T>G | NCBI36 |
NG_012046.2:g.14040A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000646379.1:c.-460+8923A>C | ENSP00000494381.1:n.-460+8923A>C | |
ENST00000397077.5:c.-460+8923A>C | ENSP00000380267.1:n.-460+8923A>C | |
XM_006713175.2:c.-460+8923A>C | XP_006713238.1:n.-460+8923A>C | |
XM_011533751.1:c.-556+8923A>C | XP_011532053.1:n.-556+8923A>C | |
XM_006713175.4:c.-460+8923A>C | XP_006713238.1:n.-460+8923A>C | |
XM_017006484.2:c.-460+8923A>C | XP_016861973.1:n.-460+8923A>C | |
XM_017006487.1:c.-460+8923A>C | XP_016861976.1:n.-460+8923A>C |