HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94030979_94030980delinsAC , CM000663.2:g.94030979_94030980delinsAC | GRCh38 |
NC_000001.10:g.94496535_94496536delinsAC , CM000663.1:g.94496535_94496536delinsAC | GRCh37 |
NC_000001.9:g.94269123_94269124delinsAC | NCBI36 |
NG_009073.1:g.95170_95171delinsGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.4253+16_4253+17delinsGT MANE Select | ENSP00000359245.3:n.4253+16_4253+17delins... | |
ENST00000370225.3:c.4253+16_4253+17delinsGT | ENSP00000359245.3:n.4253+16_4253+17delins... | |
ENST00000536513.5:c.629+16_629+17delinsGT | ENSP00000439707.2:n.629+16_629+17delinsGT... | |
NM_000350.2:c.4253+16_4253+17delinsGT | NP_000341.2:n.4253+16_4253+17delinsGT | |
NM_000350.3:c.4253+16_4253+17delinsGT MANE Select | NP_000341.2:n.4253+16_4253+17delinsGT |