HGVS | Genome Assembly |
---|---|
NC_000006.12:g.26065393A>T , CM000668.2:g.26065393A>T | GRCh38 |
NC_000006.11:g.26065621A>T , CM000668.1:g.26065621A>T | GRCh37 |
NC_000006.10:g.26173600A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000629531.1:c.133-21868T>A | ENSP00000486472.1:n.133-21868T>A |