HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215799234_215799235insA , CM000663.2:g.215799234_215799235insA | GRCh38 |
NC_000001.10:g.215972576_215972577insA , CM000663.1:g.215972576_215972577insA | GRCh37 |
NC_000001.9:g.214039199_214039200insA | NCBI36 |
NG_009497.1:g.629162_629163insT | |
NG_009497.2:g.629214_629215insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.9740-110_9740-109insT MANE Select | ENSP00000305941.3:n.9740-110_9740-109insT | |
ENST00000674083.1:c.9740-110_9740-109insT | ENSP00000501296.1:n.9740-110_9740-109insT | |
ENST00000307340.7:c.9740-110_9740-109insT | ENSP00000305941.3:n.9740-110_9740-109insT | |
NM_206933.2:c.9740-110_9740-109insT | NP_996816.2:n.9740-110_9740-109insT | |
NM_206933.3:c.9740-110_9740-109insT | NP_996816.2:n.9740-110_9740-109insT | |
NM_206933.4:c.9740-110_9740-109insT MANE Select | NP_996816.3:n.9740-110_9740-109insT |