HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21176684_21176689del , CM000674.2:g.21176684_21176689del | GRCh38 |
NC_000012.11:g.21329618_21329623del , CM000674.1:g.21329618_21329623del | GRCh37 |
NC_000012.10:g.21220885_21220890del | NCBI36 |
NG_011745.1:g.50491_50496del , LRG_1022:g.50491_50496del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.360-92_360-87del MANE Select | ENSP00000256958.2:n.360-92_360-87del | |
ENST00000256958.2:c.360-92_360-87del | ENSP00000256958.2:n.360-92_360-87del | |
ENST00000543498.5:c.426-92_426-87del | ||
NM_006446.4:c.360-92_360-87del , LRG_1022t1:c.360-92_360-87del | NP_006437.3:n.360-92_360-87del | |
NM_006446.5:c.360-92_360-87del MANE Select | NP_006437.3:n.360-92_360-87del |