HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151526670_151526671delinsGC , CM000668.2:g.151526670_151526671delinsGC | GRCh38 |
NC_000006.11:g.151847805_151847806delinsGC , CM000668.1:g.151847805_151847806delinsGC | GRCh37 |
NC_000006.10:g.151889498_151889499delinsGC | NCBI36 |
NG_021198.1:g.37631_37632delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239374.8:c.58-9648_58-9647delinsGC MANE Select | ENSP00000239374.6:n.58-9648_58-9647delinsGC | |
ENST00000239374.7:c.58-9648_58-9647delinsGC | ENSP00000239374.6:n.58-9648_58-9647delinsGC | |
NM_025059.3:c.58-9648_58-9647delinsGC | NP_079335.2:n.58-9648_58-9647delinsGC | |
NM_025059.4:c.58-9648_58-9647delinsGC MANE Select | NP_079335.2:n.58-9648_58-9647delinsGC |