HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62528599T= , CM000672.2:g.62528599T= | GRCh38 |
NC_000010.10:g.64288358T= , CM000672.1:g.64288358T= | GRCh37 |
NC_000010.9:g.63958364T= | NCBI36 |
NG_021209.1:g.159443T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647733.1:c.981+68802T= | ENSP00000502188.1:n.981+68802T= | |
ENST00000395251.5:c.-185+8002T= | ENSP00000378672.1:n.-185+8002T= | |
ENST00000410046.7:c.981+68802T= | ENSP00000387091.3:n.981+68802T= | |
NM_199451.2:c.981+68802T= | NP_955523.1:n.981+68802T= | |
NM_199452.3:c.-185+8002T= | NP_955524.3:n.-185+8002T= | |
XM_017015937.2:c.982-15610T= | XP_016871426.1:n.982-15610T= | |
NM_199451.3:c.981+68802T= | NP_955523.1:n.981+68802T= |