HGVS | Genome Assembly |
---|---|
NC_000010.11:g.100045491del , CM000672.2:g.100045491del | GRCh38 |
NC_000010.10:g.101805248del , CM000672.1:g.101805248del | GRCh37 |
NC_000010.9:g.101795238del | NCBI36 |
NG_012060.1:g.41397del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370418.8:c.1231-2916del MANE Select | ENSP00000359446.3:n.1231-2916del | |
ENST00000370418.7:c.1231-2916del | ENSP00000359446.3:n.1231-2916del | |
NM_001308.2:c.1231-2916del | NP_001299.1:n.1231-2916del | |
XM_011539299.1:c.1273-2916del | XP_011537601.1:n.1273-2916del | |
NM_001308.3:c.1231-2916del MANE Select | NP_001299.1:n.1231-2916del |