HGVS | Genome Assembly |
---|---|
NC_000003.12:g.147413334_147413335insT , CM000665.2:g.147413334_147413335insT | GRCh38 |
NC_000003.11:g.147131121_147131122insT , CM000665.1:g.147131121_147131122insT | GRCh37 |
NC_000003.10:g.148613811_148613812insT | NCBI36 |
NG_015886.1:g.8941_8942insT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000282928.5:c.1147-20_1147-19insT MANE Select | ENSP00000282928.4:n.1147-20_1147-19insT | |
ENST00000282928.4:c.1147-20_1147-19insT | ENSP00000282928.4:n.1147-20_1147-19insT | |
ENST00000472523.1:n.521+19392_521+19393insT | ||
ENST00000488404.5:c.213-20_213-19insT | ||
NM_003412.3:c.1147-20_1147-19insT | NP_003403.2:n.1147-20_1147-19insT | |
NM_003412.4:c.1147-20_1147-19insT MANE Select | NP_003403.2:n.1147-20_1147-19insT |