HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215853_21215857delinsTAGGC , CM000674.2:g.21215853_21215857delinsTAGGC | GRCh38 |
NC_000012.11:g.21368787_21368791delinsTAGGC , CM000674.1:g.21368787_21368791delinsTAGGC | GRCh37 |
NC_000012.10:g.21260054_21260058delinsTAGGC | NCBI36 |
NG_011745.1:g.89660_89664delinsTAGGC , LRG_1022:g.89660_89664delinsTAGGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1266_1498-1262delinsTAGGC MANE Select | ENSP00000256958.2:n.1498-1266_1498-1262de... | |
ENST00000256958.2:c.1498-1266_1498-1262delinsTAGGC | ENSP00000256958.2:n.1498-1266_1498-1262de... | |
NM_006446.4:c.1498-1266_1498-1262delinsTAGGC , LRG_1022t1:c.1498-1266_1498-1262delinsTAGGC | NP_006437.3:n.1498-1266_1498-1262delinsTA... | |
NM_006446.5:c.1498-1266_1498-1262delinsTAGGC MANE Select | NP_006437.3:n.1498-1266_1498-1262delinsTA... |