HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147882766G= , CM000669.2:g.147882766G= | GRCh38 |
NC_000007.13:g.147579858G= , CM000669.1:g.147579858G= | GRCh37 |
NC_000007.12:g.147210791G= | NCBI36 |
NG_007092.2:g.1771406G= | |
NG_007092.3:g.1771766G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.2099-20799G= MANE Select | ENSP00000354778.3:n.2099-20799G= | |
ENST00000636870.1:n.1961-20799G= | ||
ENST00000637825.1:n.1582-20799G= | ||
ENST00000361727.7:c.2099-20799G= | ENSP00000354778.3:n.2099-20799G= | |
ENST00000455301.2:n.34-20799G= | ||
ENST00000627772.2:n.272-20799G= | ||
NM_014141.5:c.2099-20799G= | NP_054860.1:n.2099-20799G= | |
XM_006715919.1:c.587-20799G= | XP_006715982.1:n.587-20799G= | |
NM_014141.6:c.2099-20799G= MANE Select | NP_054860.1:n.2099-20799G= |