HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47333812del , CM000673.2:g.47333812del | GRCh38 |
NC_000011.9:g.47355363del , CM000673.1:g.47355363del | GRCh37 |
NC_000011.8:g.47311939del | NCBI36 |
NG_007667.1:g.23894del , LRG_386:g.23894del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.2995-57del MANE Select | ENSP00000442795.1:n.2995-57del | |
ENST00000256993.8:c.2995-57del | ENSP00000256993.5:n.2995-57del | |
ENST00000399249.6:c.2995-57del | ENSP00000382193.2:n.2995-57del | |
ENST00000545968.5:c.2995-57del | ENSP00000442795.1:n.2995-57del | |
NM_000256.3:c.2995-57del , LRG_386t1:c.2995-57del MANE Select | NP_000247.2:n.2995-57del | |
XM_011520117.1:c.2977-57del | XP_011518419.1:n.2977-57del | |
XM_011520118.1:c.2914-57del | XP_011518420.1:n.2914-57del |