HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584073_41584074insCA , CM000679.2:g.41584073_41584074insCA | GRCh38 |
NC_000017.10:g.39740325_39740326insCA , CM000679.1:g.39740325_39740326insCA | GRCh37 |
NC_000017.9:g.36993851_36993852insCA | NCBI36 |
NG_008624.1:g.7822_7823insTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-153_766-152insTG MANE Select | ENSP00000167586.6:n.766-153_766-152insTG | |
ENST00000167586.6:c.766-153_766-152insTG | ENSP00000167586.6:n.766-153_766-152insTG | |
ENST00000476662.1:n.216-153_216-152insTG | ||
NM_000526.4:c.766-153_766-152insTG | NP_000517.2:n.766-153_766-152insTG | |
NM_000526.5:c.766-153_766-152insTG MANE Select | NP_000517.3:n.766-153_766-152insTG |