HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94062532_94062535dup , CM000663.2:g.94062532_94062535dup | GRCh38 |
NC_000001.10:g.94528088_94528091dup , CM000663.1:g.94528088_94528091dup | GRCh37 |
NC_000001.9:g.94300676_94300679dup | NCBI36 |
NG_009073.1:g.63616_63619dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.1937+43_1937+46dup MANE Select | ENSP00000359245.3:n.1937+43_1937+46dup | |
ENST00000649773.1:c.1937+43_1937+46dup | ENSP00000496882.1:n.1937+43_1937+46dup | |
ENST00000370225.3:c.1937+43_1937+46dup | ENSP00000359245.3:n.1937+43_1937+46dup | |
ENST00000536513.5:c.-65+640_-65+643dup | ENSP00000439707.2:n.-65+640_-65+643dup | |
NM_000350.2:c.1937+43_1937+46dup | NP_000341.2:n.1937+43_1937+46dup | |
NM_000350.3:c.1937+43_1937+46dup MANE Select | NP_000341.2:n.1937+43_1937+46dup |