HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71941916_71941917delinsGC , CM000674.2:g.71941916_71941917delinsGC | GRCh38 |
NC_000012.11:g.72335696_72335697delinsGC , CM000674.1:g.72335696_72335697delinsGC | GRCh37 |
NC_000012.10:g.70621963_70621964delinsGC | NCBI36 |
NG_008279.1:g.8071_8072delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000333850.4:c.255+183_255+184delinsGC MANE Select | ENSP00000329093.3:n.255+183_255+184delinsGC | |
ENST00000333850.3:c.255+183_255+184delinsGC | ENSP00000329093.3:n.255+183_255+184delinsGC | |
ENST00000546576.1:n.265+183_265+184delinsGC | ||
NM_173353.3:c.255+183_255+184delinsGC | NP_775489.2:n.255+183_255+184delinsGC | |
XR_245894.2:n.355+183_355+184delinsGC | ||
XR_001748575.1:n.355+183_355+184delinsGC | ||
NM_173353.4:c.255+183_255+184delinsGC MANE Select | NP_775489.2:n.255+183_255+184delinsGC |