HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32636527T>C , CM000668.2:g.32636527T>C | GRCh38 |
NC_000006.11:g.32604304T>C , CM000668.1:g.32604304T>C | GRCh37 |
NC_000006.10:g.32712282T>C | NCBI36 |
NG_032876.1:g.4122T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000422863.1:c.-38-894T>C | ENSP00000405797.1:n.-38-894T>C |