HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111072229_111072242del , CM000667.2:g.111072229_111072242del | GRCh38 |
NC_000005.9:g.110407927_110407940del , CM000667.1:g.110407927_110407940del | GRCh37 |
NC_000005.8:g.110435826_110435839del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344895.4:c.171+168_171+181del MANE Select | ENSP00000339804.3:n.171+168_171+181del | |
ENST00000344895.3:c.171+168_171+181del | ENSP00000339804.3:n.171+168_171+181del | |
ENST00000420978.6:c.171+168_171+181del | ENSP00000399099.2:n.171+168_171+181del | |
NM_033035.4:c.171+168_171+181del | NP_149024.1:n.171+168_171+181del | |
NR_045089.1:n.1575+168_1575+181del | ||
NM_033035.5:c.171+168_171+181del MANE Select | NP_149024.1:n.171+168_171+181del | |
NR_045089.2:n.1593+168_1593+181del |