HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869100_240869102delinsGA , CM000664.2:g.240869100_240869102delinsGA | GRCh38 |
NC_000002.11:g.241808517_241808519delinsGA , CM000664.1:g.241808517_241808519delinsGA | GRCh37 |
NC_000002.10:g.241457190_241457192delinsGA | NCBI36 |
NG_008005.1:g.5356_5358delinsGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.166-70_166-68delinsGA MANE Select | ENSP00000302620.3:n.166-70_166-68delinsGA... | |
ENST00000307503.3:c.166-70_166-68delinsGA | ENSP00000302620.3:n.166-70_166-68delinsGA... | |
ENST00000472436.1:n.186-70_186-68delinsGA | ||
NM_000030.2:c.166-70_166-68delinsGA | NP_000021.1:n.166-70_166-68delinsGA | |
XR_924060.1:n.405+1131_405+1133delinsTC | ||
NM_000030.3:c.166-70_166-68delinsGA MANE Select | NP_000021.1:n.166-70_166-68delinsGA |