HGVS | Genome Assembly |
---|---|
NC_000006.12:g.117450116G>A , CM000668.2:g.117450116G>A | GRCh38 |
NC_000006.11:g.117771279G>A , CM000668.1:g.117771279G>A | GRCh37 |
NC_000006.10:g.117877972G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000467125.1:c.547+116738C>T | ENSP00000487717.1:n.547+116738C>T |