HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44305210_44305211insTT , CM000667.2:g.44305210_44305211insTT | GRCh38 |
NC_000005.9:g.44305312_44305313insTT , CM000667.1:g.44305312_44305313insTT | GRCh37 |
NC_000005.8:g.44341069_44341070insTT | NCBI36 |
NG_011446.1:g.88472_88473insAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.430-19_430-18insAA MANE Select | ENSP00000264664.4:n.430-19_430-18insAA | |
ENST00000264664.4:c.430-19_430-18insAA | ENSP00000264664.4:n.430-19_430-18insAA | |
NM_004465.1:c.430-19_430-18insAA | NP_004456.1:n.430-19_430-18insAA | |
XM_005248264.2:c.430-19_430-18insAA | XP_005248321.1:n.430-19_430-18insAA | |
XM_005248264.4:c.430-19_430-18insAA | XP_005248321.1:n.430-19_430-18insAA | |
NM_004465.2:c.430-19_430-18insAA MANE Select | NP_004456.1:n.430-19_430-18insAA |