HGVS | Genome Assembly |
---|---|
NC_000003.12:g.147413296_147413297del , CM000665.2:g.147413296_147413297del | GRCh38 |
NC_000003.11:g.147131083_147131084del , CM000665.1:g.147131083_147131084del | GRCh37 |
NC_000003.10:g.148613773_148613774del | NCBI36 |
NG_015886.1:g.8903_8904del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000282928.5:c.1147-58_1147-57del MANE Select | ENSP00000282928.4:n.1147-58_1147-57del | |
ENST00000282928.4:c.1147-58_1147-57del | ENSP00000282928.4:n.1147-58_1147-57del | |
ENST00000472523.1:n.521+19354_521+19355del | ||
ENST00000488404.5:c.213-58_213-57del | ||
NM_003412.3:c.1147-58_1147-57del | NP_003403.2:n.1147-58_1147-57del | |
NM_003412.4:c.1147-58_1147-57del MANE Select | NP_003403.2:n.1147-58_1147-57del |