HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240872934_240872943delinsCCCTGCCTCA , CM000664.2:g.240872934_240872943delinsCCCTGCCTCA | GRCh38 |
NC_000002.11:g.241812351_241812360delinsCCCTGCCTCA , CM000664.1:g.241812351_241812360delinsCCCTGCCTCA | GRCh37 |
NC_000002.10:g.241461024_241461033delinsCCCTGCCTCA | NCBI36 |
NG_008005.1:g.9190_9199delinsCCCTGCCTCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.525-45_525-36delinsCCCTGCCTCA MANE Select | ENSP00000302620.3:n.525-45_525-36delinsCC... | |
ENST00000307503.3:c.525-45_525-36delinsCCCTGCCTCA | ENSP00000302620.3:n.525-45_525-36delinsCC... | |
ENST00000472436.1:n.545-45_545-36delinsCCCTGCCTCA | ||
ENST00000476698.1:n.262-45_262-36delinsCCCTGCCTCA | ||
NM_000030.2:c.525-45_525-36delinsCCCTGCCTCA | NP_000021.1:n.525-45_525-36delinsCCCTGCCT... | |
NM_000030.3:c.525-45_525-36delinsCCCTGCCTCA MANE Select | NP_000021.1:n.525-45_525-36delinsCCCTGCCT... |