HGVS | Genome Assembly |
---|---|
NC_000016.10:g.8797742T= , CM000678.2:g.8797742T= | GRCh38 |
NC_000016.9:g.8891599T= , CM000678.1:g.8891599T= | GRCh37 |
NC_000016.8:g.8799100T= | NCBI36 |
NG_009209.1:g.4930T= | |
NG_033146.1:g.4907A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682008.1:c.-141T= | ENSP00000507849.1:n.-141T= | |
ENST00000566983.5:c.-15-4057T= | ENSP00000457956.1:n.-15-4057T= |