HGVS | Genome Assembly |
---|---|
NC_000006.12:g.160668449T>C , CM000668.2:g.160668449T>C | GRCh38 |
NC_000006.11:g.161089481T>C , CM000668.1:g.161089481T>C | GRCh37 |
NC_000006.10:g.161009471T>C | NCBI36 |
NG_016147.1:g.2927A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000452651.1:n.115-2076A>G |