HGVS | Genome Assembly |
---|---|
NC_000006.12:g.117450121T= , CM000668.2:g.117450121T= | GRCh38 |
NC_000006.11:g.117771284T= , CM000668.1:g.117771284T= | GRCh37 |
NC_000006.10:g.117877977T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000467125.1:c.547+116733A= | ENSP00000487717.1:n.547+116733A= |