HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423443_23423444delinsAC , CM000676.2:g.23423443_23423444delinsAC | GRCh38 |
NC_000014.8:g.23892652_23892653delinsAC , CM000676.1:g.23892652_23892653delinsAC | GRCh37 |
NC_000014.7:g.22962492_22962493delinsAC | NCBI36 |
NG_007884.1:g.17218_17219delinsGT , LRG_384:g.17218_17219delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+103_3099+104delinsGT MANE Select | ENSP00000347507.3:n.3099+103_3099+104delinsGT | |
ENST00000355349.3:c.3099+103_3099+104delinsGT | ENSP00000347507.3:n.3099+103_3099+104delinsGT | |
NM_000257.3:c.3099+103_3099+104delinsGT | NP_000248.2:n.3099+103_3099+104delinsGT | |
XR_245686.3:n.3205+103_3205+104delinsGT | ||
XM_017021340.1:c.3099+103_3099+104delinsGT | XP_016876829.1:n.3099+103_3099+104delinsGT | |
NM_000257.4:c.3099+103_3099+104delinsGT MANE Select | NP_000248.2:n.3099+103_3099+104delinsGT |