HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154905031_154905032delinsAC , CM000685.2:g.154905031_154905032delinsAC | GRCh38 |
NC_000023.10:g.154133306_154133307delinsAC , CM000685.1:g.154133306_154133307delinsAC | GRCh37 |
NC_000023.9:g.153786500_153786501delinsAC | NCBI36 |
NG_011403.1:g.122692_122693delinsGT | |
NG_011403.2:g.122692_122693delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5374-9_5374-8delinsGT MANE Select | ENSP00000353393.4:n.5374-9_5374-8delinsGT | |
ENST00000360256.8:c.5374-9_5374-8delinsGT | ENSP00000353393.4:n.5374-9_5374-8delinsGT | |
NM_000132.3:c.5374-9_5374-8delinsGT | NP_000123.1:n.5374-9_5374-8delinsGT | |
XM_011531126.1:c.5269-9_5269-8delinsGT | XP_011529428.1:n.5269-9_5269-8delinsGT | |
NM_000132.4:c.5374-9_5374-8delinsGT MANE Select | NP_000123.1:n.5374-9_5374-8delinsGT |