HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003927_47003928insCC , CM000681.2:g.47003927_47003928insCC | GRCh38 |
NC_000019.9:g.47507184_47507185insCC , CM000681.1:g.47507184_47507185insCC | GRCh37 |
NC_000019.8:g.52199024_52199025insCC | NCBI36 |
NG_047014.1:g.90361_90362insCC | |
NG_047014.2:g.147931_147932insCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7739_7740insCC | ENSP00000385720.2:n.7739_7740insCC | |
ENST00000672722.1:c.*3239_*3240insCC MANE Select | ENSP00000500409.1:n.*3239_*3240insCC | |
ENST00000404338.7:c.7739_7740insCC | ENSP00000385720.2:n.7739_7740insCC | |
ENST00000614079.1:c.7316_7317insCC | ENSP00000483730.1:n.7316_7317insCC | |
NM_004491.4:c.7739_7740insCC | NP_004482.4:n.7739_7740insCC | |
NM_004491.5:c.*3239_*3240insCC MANE Select | NP_004482.4:n.*3239_*3240insCC |