HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071780_111071781del , CM000667.2:g.111071780_111071781del | GRCh38 |
NC_000005.9:g.110407478_110407479del , CM000667.1:g.110407478_110407479del | GRCh37 |
NC_000005.8:g.110435377_110435378del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-111_-110del MANE Select | ENSP00000339804.3:n.-111_-110del | |
ENST00000344895.3:c.-111_-110del | ENSP00000339804.3:n.-111_-110del | |
ENST00000420978.6:c.35-145_35-144del | ENSP00000399099.2:n.35-145_35-144del | |
NM_033035.4:c.-111_-110del | NP_149024.1:n.-111_-110del | |
NR_045089.1:n.1439-145_1439-144del | ||
NM_033035.5:c.-111_-110del MANE Select | NP_149024.1:n.-111_-110del | |
NR_045089.2:n.1457-145_1457-144del |