HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32644638T= , CM000668.2:g.32644638T= | GRCh38 |
NC_000006.11:g.32612415T= , CM000668.1:g.32612415T= | GRCh37 |
NC_000006.10:g.32720393T= | NCBI36 |
NG_032876.1:g.12233T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460633.1:n.3026T= | ||
XM_006715079.2:c.613+2385T= | XP_006715142.1:n.613+2385T= | |
XM_006715079.4:c.613+2385T= | XP_006715142.1:n.613+2385T= |