HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32644619T= , CM000668.2:g.32644619T= | GRCh38 |
NC_000006.11:g.32612396T= , CM000668.1:g.32612396T= | GRCh37 |
NC_000006.10:g.32720374T= | NCBI36 |
NG_032876.1:g.12214T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460633.1:n.3007T= | ||
XM_006715079.2:c.613+2366T= | XP_006715142.1:n.613+2366T= | |
XM_006715079.4:c.613+2366T= | XP_006715142.1:n.613+2366T= |