HGVS | Genome Assembly |
---|---|
NC_000010.11:g.46046553T= , CM000672.2:g.46046553T= | GRCh38 |
NC_000010.10:g.51549269A= , CM000672.1:g.51549269A= | GRCh37 |
NC_000010.9:g.51219275A= | NCBI36 |
NG_011551.1:g.4717A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000663171.1:c.-142-174A= | ENSP00000499419.1:n.-142-174A= |