HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071738_111071743del , CM000667.2:g.111071738_111071743del | GRCh38 |
NC_000005.9:g.110407436_110407441del , CM000667.1:g.110407436_110407441del | GRCh37 |
NC_000005.8:g.110435335_110435340del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-153_-148del MANE Select | ENSP00000339804.3:n.-153_-148del | |
ENST00000344895.3:c.-153_-148del | ENSP00000339804.3:n.-153_-148del | |
ENST00000420978.6:c.35-187_35-182del | ENSP00000399099.2:n.35-187_35-182del | |
NM_033035.4:c.-153_-148del | NP_149024.1:n.-153_-148del | |
NR_045089.1:n.1439-187_1439-182del | ||
NM_033035.5:c.-153_-148del MANE Select | NP_149024.1:n.-153_-148del | |
NR_045089.2:n.1457-187_1457-182del |