HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62610549C>T , CM000672.2:g.62610549C>T | GRCh38 |
NC_000010.10:g.64370308C>T , CM000672.1:g.64370308C>T | GRCh37 |
NC_000010.9:g.64040314C>T | NCBI36 |
NG_021209.1:g.241393C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647733.1:c.982-12554C>T | ENSP00000502188.1:n.982-12554C>T | |
ENST00000395251.5:c.-184-33193C>T | ENSP00000378672.1:n.-184-33193C>T | |
ENST00000410046.7:c.982-12554C>T | ENSP00000387091.3:n.982-12554C>T | |
NM_199451.2:c.982-12554C>T | NP_955523.1:n.982-12554C>T | |
NM_199452.3:c.-184-33193C>T | NP_955524.3:n.-184-33193C>T | |
NM_199451.3:c.982-12554C>T | NP_955523.1:n.982-12554C>T |