HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135859148_135859149delinsCT , CM000664.2:g.135859148_135859149delinsCT | GRCh38 |
NC_000002.11:g.136616718_136616719delinsCT , CM000664.1:g.136616718_136616719delinsCT | GRCh37 |
NC_000002.10:g.136333188_136333189delinsCT | NCBI36 |
NG_008104.2:g.1021_1022delinsAG , LRG_338:g.1021_1022delinsAG | |
NG_008958.1:g.22293_22294delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1362+152_1362+153delinsAG MANE Select | ENSP00000264156.2:n.1362+152_1362+153delinsAG | |
ENST00000264156.2:c.1362+152_1362+153delinsAG | ENSP00000264156.2:n.1362+152_1362+153delinsAG | |
ENST00000492091.1:n.181+3458_181+3459delinsAG | ||
NM_005915.5:c.1362+152_1362+153delinsAG | NP_005906.2:n.1362+152_1362+153delinsAG | |
NM_005915.6:c.1362+152_1362+153delinsAG MANE Select | NP_005906.2:n.1362+152_1362+153delinsAG |