HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202654_32202656delinsTCC , CM000668.2:g.32202654_32202656delinsTCC | GRCh38 |
NC_000006.11:g.32170431_32170433delinsTCC , CM000668.1:g.32170431_32170433delinsTCC | GRCh37 |
NC_000006.10:g.32278409_32278411delinsTCC | NCBI36 |
NG_028190.1:g.26412_26414delinsGGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375023.3:c.3232-57_3232-55delinsGGA MANE Select | ENSP00000364163.3:n.3232-57_3232-55delins... | |
ENST00000474612.1:n.1261_1263delinsGGA | ||
NM_004557.3:c.3232-57_3232-55delinsGGA | NP_004548.3:n.3232-57_3232-55delinsGGA | |
NR_134949.1:n.3472+1114_3472+1116delinsGGA | ||
NR_134950.1:n.3370+1114_3370+1116delinsGGA | ||
NM_004557.4:c.3232-57_3232-55delinsGGA MANE Select | NP_004548.3:n.3232-57_3232-55delinsGGA | |
NR_134949.2:n.3472+1114_3472+1116delinsGGA | ||
NR_134950.2:n.3370+1114_3370+1116delinsGGA |