HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32634531T>C , CM000668.2:g.32634531T>C | GRCh38 |
NC_000006.11:g.32602308T>C , CM000668.1:g.32602308T>C | GRCh37 |
NC_000006.10:g.32710286T>C | NCBI36 |
NG_032876.1:g.2126T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000422863.1:c.-39+1622T>C | ENSP00000405797.1:n.-39+1622T>C |