HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736663_153736664delinsGC , CM000685.2:g.153736663_153736664delinsGC | GRCh38 |
NC_000023.10:g.153002117_153002118delinsGC , CM000685.1:g.153002117_153002118delinsGC | GRCh37 |
NC_000023.9:g.152655311_152655312delinsGC | NCBI36 |
NG_009022.2:g.16796_16797delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1393+150_1393+151delinsGC MANE Select | ENSP00000218104.3:n.1393+150_1393+151delinsGC | |
ENST00000218104.5:c.1393+150_1393+151delinsGC | ENSP00000218104.3:n.1393+150_1393+151delinsGC | |
ENST00000443684.2:n.396+150_396+151delinsGC | ||
NM_000033.3:c.1393+150_1393+151delinsGC | NP_000024.2:n.1393+150_1393+151delinsGC | |
XR_938507.1:n.1809+150_1809+151delinsGC | ||
XR_938507.2:n.1809+150_1809+151delinsGC | ||
NM_000033.4:c.1393+150_1393+151delinsGC MANE Select | NP_000024.2:n.1393+150_1393+151delinsGC |