HGVS | Genome Assembly |
---|---|
NC_000002.12:g.232523687del , CM000664.2:g.232523687del | GRCh38 |
NC_000002.11:g.233388397del , CM000664.1:g.233388397del | GRCh37 |
NC_000002.10:g.233096641del | NCBI36 |
NG_008028.1:g.2476del | |
NG_031969.1:g.8225del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000617714.2:c.1013-85del MANE Select | ENSP00000479745.1:n.1013-85del | |
ENST00000449534.6:c.1013-82del | ENSP00000473410.1:n.1013-82del | |
ENST00000617714.1:c.1013-85del | ENSP00000479745.1:n.1013-85del | |
NM_001195129.1:c.1013-85del | NP_001182058.1:n.1013-85del | |
NM_001195129.2:c.1013-85del MANE Select | NP_001182058.1:n.1013-85del | |
NM_001369848.1:c.1013-82del | NP_001356777.1:n.1013-82del |