HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69647773_69647774del , CM000673.2:g.69647773_69647774del | GRCh38 |
NC_000011.9:g.69462541_69462542del , CM000673.1:g.69462541_69462542del | GRCh37 |
NC_000011.8:g.69171722_69171723del | NCBI36 |
NG_007375.1:g.11669_11670del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227507.3:c.575-221_575-220del MANE Select | ENSP00000227507.2:n.575-221_575-220del | |
ENST00000227507.2:c.575-221_575-220del | ENSP00000227507.2:n.575-221_575-220del | |
ENST00000536559.1:c.199-221_199-220del | ENSP00000438482.1:n.199-221_199-220del | |
ENST00000545484.1:n.281-221_281-220del | ||
NM_053056.2:c.575-221_575-220del | NP_444284.1:n.575-221_575-220del | |
XM_006718653.2:c.599-221_599-220del | XP_006718716.1:n.599-221_599-220del | |
NM_053056.3:c.575-221_575-220del MANE Select | NP_444284.1:n.575-221_575-220del |