HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49130868_49130869insT , CM000665.2:g.49130868_49130869insT | GRCh38 |
NC_000003.11:g.49168301_49168302insT , CM000665.1:g.49168301_49168302insT | GRCh37 |
NC_000003.10:g.49143305_49143306insT | NCBI36 |
NG_008094.1:g.7298_7299insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305544.9:c.916-9_916-8insA MANE Select | ENSP00000307156.4:n.916-9_916-8insA | |
ENST00000305544.8:c.916-9_916-8insA | ENSP00000307156.4:n.916-9_916-8insA | |
ENST00000418109.5:c.916-9_916-8insA | ENSP00000388325.1:n.916-9_916-8insA | |
NM_002292.3:c.916-9_916-8insA | NP_002283.3:n.916-9_916-8insA | |
XM_005265127.3:c.916-9_916-8insA | XP_005265184.1:n.916-9_916-8insA | |
XM_005265127.4:c.916-9_916-8insA | XP_005265184.1:n.916-9_916-8insA | |
NM_002292.4:c.916-9_916-8insA MANE Select | NP_002283.3:n.916-9_916-8insA |