HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739806_86739816del , CM000670.2:g.86739806_86739816del | GRCh38 |
NC_000008.10:g.87752034_87752044del , CM000670.1:g.87752034_87752044del | GRCh37 |
NC_000008.9:g.87821150_87821160del | NCBI36 |
NG_016980.1:g.8860_8870del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.130-80_130-70del MANE Select | ENSP00000316605.5:n.130-80_130-70del | |
ENST00000681746.1:c.130-80_130-70del | ENSP00000505959.1:n.130-80_130-70del | |
ENST00000320005.5:c.130-80_130-70del | ENSP00000316605.5:n.130-80_130-70del | |
ENST00000519777.1:n.112-80_112-70del | ||
NM_019098.4:c.130-80_130-70del | NP_061971.3:n.130-80_130-70del | |
NM_019098.5:c.130-80_130-70del MANE Select | NP_061971.3:n.130-80_130-70del |