HGVS | Genome Assembly |
---|---|
NC_000001.11:g.10973157_10973158delinsGA , CM000663.2:g.10973157_10973158delinsGA | GRCh38 |
NC_000001.10:g.11033214_11033215delinsGA , CM000663.1:g.11033214_11033215delinsGA | GRCh37 |
NC_000001.9:g.10955801_10955802delinsGA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000377004.9:c.127+2998_127+2999delinsTC MANE Select | ENSP00000366203.4:n.127+2998_127+2999deli... | |
ENST00000377004.8:c.127+2998_127+2999delinsTC | ENSP00000366203.4:n.127+2998_127+2999deli... | |
ENST00000520253.1:c.60+2998_60+2999delinsTC | ||
NM_001170754.1:c.127+2998_127+2999delinsTC | NP_001164225.1:n.127+2998_127+2999delinsT... | |
NM_001170754.2:c.127+2998_127+2999delinsTC MANE Select | NP_001164225.1:n.127+2998_127+2999delinsT... |