HGVS | Genome Assembly |
---|---|
NC_000006.12:g.112069704T>C , CM000668.2:g.112069704T>C | GRCh38 |
NC_000006.11:g.112390907T>C , CM000668.1:g.112390907T>C | GRCh37 |
NC_000006.10:g.112497600T>C | NCBI36 |
NG_011748.1:g.20630T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361714.5:c.*84T>C | ENSP00000354734.2:n.*84T>C | |
ENST00000368666.6:c.*84T>C | ENSP00000357655.3:n.*84T>C |