HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927696_149927697delinsGC , CM000663.2:g.149927696_149927697delinsGC | GRCh38 |
NC_000001.10:g.149899588_149899589delinsGC , CM000663.1:g.149899588_149899589delinsGC | GRCh37 |
NC_000001.9:g.148166212_148166213delinsGC | NCBI36 |
NG_032777.1:g.5556_5557delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.34+29_34+30delinsGC MANE Select | ENSP00000271628.8:n.34+29_34+30delinsGC | |
ENST00000271628.8:c.34+29_34+30delinsGC | ENSP00000271628.8:n.34+29_34+30delinsGC | |
NM_005850.4:c.34+29_34+30delinsGC | NP_005841.1:n.34+29_34+30delinsGC | |
NM_005850.5:c.34+29_34+30delinsGC MANE Select | NP_005841.1:n.34+29_34+30delinsGC |