HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584422_41584425delinsACCC , CM000679.2:g.41584422_41584425delinsACCC | GRCh38 |
NC_000017.10:g.39740674_39740677delinsACCC , CM000679.1:g.39740674_39740677delinsACCC | GRCh37 |
NC_000017.9:g.36994200_36994203delinsACCC | NCBI36 |
NG_008624.1:g.7471_7474delinsGGGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000167586.7:c.609-12_609-9delinsGGGT MANE Select | ENSP00000167586.6:n.609-12_609-9delinsGGG... | |
ENST00000167586.6:c.609-12_609-9delinsGGGT | ENSP00000167586.6:n.609-12_609-9delinsGGG... | |
ENST00000476662.1:n.47_50delinsGGGT | ||
NM_000526.4:c.609-12_609-9delinsGGGT | NP_000517.2:n.609-12_609-9delinsGGGT | |
NM_000526.5:c.609-12_609-9delinsGGGT MANE Select | NP_000517.3:n.609-12_609-9delinsGGGT |