HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19961710_19961713del , CM000670.2:g.19961710_19961713del | GRCh38 |
NC_000008.10:g.19819221_19819224del , CM000670.1:g.19819221_19819224del | GRCh37 |
NC_000008.9:g.19863501_19863504del | NCBI36 |
NG_008855.1:g.27640_27643del | |
NG_008855.2:g.64994_64997del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.1323-405_1323-402del MANE Select | ENSP00000497642.1:n.1323-405_1323-402del | |
ENST00000650478.1:c.263-405_263-402del | ENSP00000497560.1:n.263-405_263-402del | |
ENST00000311322.8:c.1323-405_1323-402del | ENSP00000309757.6:n.1323-405_1323-402del | |
NM_000237.2:c.1323-405_1323-402del | NP_000228.1:n.1323-405_1323-402del | |
NM_000237.3:c.1323-405_1323-402del MANE Select | NP_000228.1:n.1323-405_1323-402del |