HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23425206_23425207delinsGC , CM000676.2:g.23425206_23425207delinsGC | GRCh38 |
NC_000014.8:g.23894415_23894416delinsGC , CM000676.1:g.23894415_23894416delinsGC | GRCh37 |
NC_000014.7:g.22964255_22964256delinsGC | NCBI36 |
NG_007884.1:g.15455_15456delinsGC , LRG_384:g.15455_15456delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2423+75_2423+76delinsGC MANE Select | ENSP00000347507.3:n.2423+75_2423+76delinsGC | |
ENST00000355349.3:c.2423+75_2423+76delinsGC | ENSP00000347507.3:n.2423+75_2423+76delinsGC | |
NM_000257.3:c.2423+75_2423+76delinsGC | NP_000248.2:n.2423+75_2423+76delinsGC | |
XR_245686.3:n.2529+75_2529+76delinsGC | ||
XM_017021340.1:c.2423+75_2423+76delinsGC | XP_016876829.1:n.2423+75_2423+76delinsGC | |
NM_000257.4:c.2423+75_2423+76delinsGC MANE Select | NP_000248.2:n.2423+75_2423+76delinsGC |