HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003917_47003918insTC , CM000681.2:g.47003917_47003918insTC | GRCh38 |
NC_000019.9:g.47507174_47507175insTC , CM000681.1:g.47507174_47507175insTC | GRCh37 |
NC_000019.8:g.52199014_52199015insTC | NCBI36 |
NG_047014.1:g.90351_90352insTC | |
NG_047014.2:g.147921_147922insTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7729_7730insTC | ENSP00000385720.2:n.7729_7730insTC | |
ENST00000672722.1:c.*3229_*3230insTC MANE Select | ENSP00000500409.1:n.*3229_*3230insTC | |
ENST00000404338.7:c.7729_7730insTC | ENSP00000385720.2:n.7729_7730insTC | |
ENST00000614079.1:c.7306_7307insTC | ENSP00000483730.1:n.7306_7307insTC | |
NM_004491.4:c.7729_7730insTC | NP_004482.4:n.7729_7730insTC | |
NM_004491.5:c.*3229_*3230insTC MANE Select | NP_004482.4:n.*3229_*3230insTC |