HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153741045_153741046delinsCT , CM000685.2:g.153741045_153741046delinsCT | GRCh38 |
NC_000023.10:g.153006499_153006500delinsCT , CM000685.1:g.153006499_153006500delinsCT | GRCh37 |
NC_000023.9:g.152659693_152659694delinsCT | NCBI36 |
NG_009022.2:g.21178_21179delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000218104.6:c.1780+326_1780+327delinsCT MANE Select | ENSP00000218104.3:n.1780+326_1780+327deli... | |
ENST00000218104.5:c.1780+326_1780+327delinsCT | ENSP00000218104.3:n.1780+326_1780+327deli... | |
NM_000033.3:c.1780+326_1780+327delinsCT | NP_000024.2:n.1780+326_1780+327delinsCT | |
XR_938507.1:n.2252+326_2252+327delinsCT | ||
XR_938507.2:n.2252+326_2252+327delinsCT | ||
NM_000033.4:c.1780+326_1780+327delinsCT MANE Select | NP_000024.2:n.1780+326_1780+327delinsCT |