HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114714010_114714011del , CM000663.2:g.114714010_114714011del | GRCh38 |
NC_000001.10:g.115256631_115256632del , CM000663.1:g.115256631_115256632del | GRCh37 |
NC_000001.9:g.115058154_115058155del | NCBI36 |
NG_007572.1:g.7885_7886del , LRG_92:g.7885_7886del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-32_112-31del MANE Select | ENSP00000358548.4:n.112-32_112-31del | |
ENST00000369535.4:c.112-32_112-31del | ENSP00000358548.4:n.112-32_112-31del | |
NM_002524.4:c.112-32_112-31del | NP_002515.1:n.112-32_112-31del | |
NM_002524.5:c.112-32_112-31del MANE Select | NP_002515.1:n.112-32_112-31del |