HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423413_23423414delinsAC , CM000676.2:g.23423413_23423414delinsAC | GRCh38 |
NC_000014.8:g.23892622_23892623delinsAC , CM000676.1:g.23892622_23892623delinsAC | GRCh37 |
NC_000014.7:g.22962462_22962463delinsAC | NCBI36 |
NG_007884.1:g.17248_17249delinsGT , LRG_384:g.17248_17249delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+133_3099+134delinsGT MANE Select | ENSP00000347507.3:n.3099+133_3099+134delinsGT | |
ENST00000355349.3:c.3099+133_3099+134delinsGT | ENSP00000347507.3:n.3099+133_3099+134delinsGT | |
NM_000257.3:c.3099+133_3099+134delinsGT | NP_000248.2:n.3099+133_3099+134delinsGT | |
XR_245686.3:n.3205+133_3205+134delinsGT | ||
XM_017021340.1:c.3099+133_3099+134delinsGT | XP_016876829.1:n.3099+133_3099+134delinsGT | |
NM_000257.4:c.3099+133_3099+134delinsGT MANE Select | NP_000248.2:n.3099+133_3099+134delinsGT |