HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071729_111071730insA , CM000667.2:g.111071729_111071730insA | GRCh38 |
NC_000005.9:g.110407427_110407428insA , CM000667.1:g.110407427_110407428insA | GRCh37 |
NC_000005.8:g.110435326_110435327insA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-162_-161insA MANE Select | ENSP00000339804.3:n.-162_-161insA | |
ENST00000344895.3:c.-162_-161insA | ENSP00000339804.3:n.-162_-161insA | |
ENST00000420978.6:c.35-196_35-195insA | ENSP00000399099.2:n.35-196_35-195insA | |
NM_033035.4:c.-162_-161insA | NP_149024.1:n.-162_-161insA | |
NR_045089.1:n.1439-196_1439-195insA | ||
NM_033035.5:c.-162_-161insA MANE Select | NP_149024.1:n.-162_-161insA | |
NR_045089.2:n.1457-196_1457-195insA |