HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120739709_120739710insT , CM000674.2:g.120739709_120739710insT | GRCh38 |
NC_000012.11:g.121177512_121177513insT , CM000674.1:g.121177512_121177513insT | GRCh37 |
NC_000012.10:g.119661895_119661896insT | NCBI36 |
NG_007991.1:g.18942_18943insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242592.9:c.*261_*262insT MANE Select | ENSP00000242592.4:n.*261_*262insT | |
ENST00000242592.8:c.*261_*262insT | ENSP00000242592.4:n.*261_*262insT | |
NM_000017.3:c.*261_*262insT | NP_000008.1:n.*261_*262insT | |
NM_001302554.1:c.*261_*262insT | NP_001289483.1:n.*261_*262insT | |
NM_000017.4:c.*261_*262insT MANE Select | NP_000008.1:n.*261_*262insT | |
NM_001302554.2:c.*261_*262insT | NP_001289483.1:n.*261_*262insT |