HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94062845_94062847del , CM000663.2:g.94062845_94062847del | GRCh38 |
NC_000001.10:g.94528401_94528403del , CM000663.1:g.94528401_94528403del | GRCh37 |
NC_000001.9:g.94300989_94300991del | NCBI36 |
NG_009073.1:g.63303_63305del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.1761-94_1761-92del MANE Select | ENSP00000359245.3:n.1761-94_1761-92del | |
ENST00000649773.1:c.1761-94_1761-92del | ENSP00000496882.1:n.1761-94_1761-92del | |
ENST00000370225.3:c.1761-94_1761-92del | ENSP00000359245.3:n.1761-94_1761-92del | |
ENST00000536513.5:c.-65+327_-65+329del | ENSP00000439707.2:n.-65+327_-65+329del | |
NM_000350.2:c.1761-94_1761-92del | NP_000341.2:n.1761-94_1761-92del | |
NM_000350.3:c.1761-94_1761-92del MANE Select | NP_000341.2:n.1761-94_1761-92del |