HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071845_111071846delinsTG , CM000667.2:g.111071845_111071846delinsTG | GRCh38 |
NC_000005.9:g.110407543_110407544delinsTG , CM000667.1:g.110407543_110407544delinsTG | GRCh37 |
NC_000005.8:g.110435442_110435443delinsTG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-46_-45delinsTG MANE Select | ENSP00000339804.3:n.-46_-45delinsTG | |
ENST00000344895.3:c.-46_-45delinsTG | ENSP00000339804.3:n.-46_-45delinsTG | |
ENST00000420978.6:c.35-80_35-79delinsTG | ENSP00000399099.2:n.35-80_35-79delinsTG | |
NM_033035.4:c.-46_-45delinsTG | NP_149024.1:n.-46_-45delinsTG | |
NR_045089.1:n.1439-80_1439-79delinsTG | ||
NM_033035.5:c.-46_-45delinsTG MANE Select | NP_149024.1:n.-46_-45delinsTG | |
NR_045089.2:n.1457-80_1457-79delinsTG |