HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69647908_69647909del , CM000673.2:g.69647908_69647909del | GRCh38 |
NC_000011.9:g.69462676_69462677del , CM000673.1:g.69462676_69462677del | GRCh37 |
NC_000011.8:g.69171857_69171858del | NCBI36 |
NG_007375.1:g.11804_11805del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227507.3:c.575-86_575-85del MANE Select | ENSP00000227507.2:n.575-86_575-85del | |
ENST00000227507.2:c.575-86_575-85del | ENSP00000227507.2:n.575-86_575-85del | |
ENST00000536559.1:c.199-86_199-85del | ENSP00000438482.1:n.199-86_199-85del | |
ENST00000545484.1:n.281-86_281-85del | ||
NM_053056.2:c.575-86_575-85del | NP_444284.1:n.575-86_575-85del | |
XM_006718653.2:c.599-86_599-85del | XP_006718716.1:n.599-86_599-85del | |
NM_053056.3:c.575-86_575-85del MANE Select | NP_444284.1:n.575-86_575-85del |