HGVS | Genome Assembly |
---|---|
NC_000015.10:g.42958181_42958182insCAGCG , CM000677.2:g.42958181_42958182insCAGCG | GRCh38 |
NC_000015.9:g.43250379_43250380insCAGCG , CM000677.1:g.43250379_43250380insCAGCG | GRCh37 |
NC_000015.8:g.41037671_41037672insCAGCG | NCBI36 |
NG_012182.1:g.152907_152908insCGCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290650.9:c.4758-92_4758-91insCGCTG MANE Select | ENSP00000290650.4:n.4758-92_4758-91insCGCTG | |
ENST00000290650.8:c.4758-92_4758-91insCGCTG | ENSP00000290650.4:n.4758-92_4758-91insCGCTG | |
NM_174916.2:c.4758-92_4758-91insCGCTG | NP_777576.1:n.4758-92_4758-91insCGCTG | |
NM_174916.3:c.4758-92_4758-91insCGCTG MANE Select | NP_777576.1:n.4758-92_4758-91insCGCTG |