HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24278003_24278004delinsGA , CM000668.2:g.24278003_24278004delinsGA | GRCh38 |
NC_000006.11:g.24278231_24278232delinsGA , CM000668.1:g.24278231_24278232delinsGA | GRCh37 |
NC_000006.10:g.24386210_24386211delinsGA | NCBI36 |
NG_012829.1:g.85049_85050delinsTC | |
NG_012829.2:g.110289_110290delinsTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378454.8:c.922+45_922+46delinsTC MANE Select | ENSP00000367715.3:n.922+45_922+46delinsTC... | |
ENST00000378454.7:c.922+45_922+46delinsTC | ENSP00000367715.3:n.922+45_922+46delinsTC... | |
NM_001195610.1:c.922+45_922+46delinsTC | NP_001182539.1:n.922+45_922+46delinsTC | |
NM_016356.4:c.922+45_922+46delinsTC | NP_057440.2:n.922+45_922+46delinsTC | |
NM_016356.5:c.922+45_922+46delinsTC MANE Select | NP_057440.2:n.922+45_922+46delinsTC | |
NM_001195610.2:c.922+45_922+46delinsTC | NP_001182539.1:n.922+45_922+46delinsTC |