HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117371_19117372insGAGGAAAG , CM000669.2:g.19117371_19117372insGAGGAAAG | GRCh38 |
NC_000007.13:g.19156994_19156995insGAGGAAAG , CM000669.1:g.19156994_19156995insGAGGAAAG | GRCh37 |
NC_000007.12:g.19123519_19123520insGAGGAAAG | NCBI36 |
NG_008114.1:g.5303_5304insTTCCTCCT | |
NG_008114.2:g.5303_5304insTTCCTCCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.-49_-48insTTCCTCCT MANE Select | ENSP00000242261.5:n.-49_-48insTTCCTCCT | |
ENST00000242261.5:c.-49_-48insTTCCTCCT | ENSP00000242261.5:n.-49_-48insTTCCTCCT | |
NM_000474.3:c.-49_-48insTTCCTCCT | NP_000465.1:n.-49_-48insTTCCTCCT | |
XM_011515496.1:c.-49_-48insTTCCTCCT | XP_011513798.1:n.-49_-48insTTCCTCCT | |
NR_149001.1:n.303_304insTTCCTCCT | ||
NM_000474.4:c.-49_-48insTTCCTCCT MANE Select | NP_000465.1:n.-49_-48insTTCCTCCT | |
NR_149001.2:n.267_268insTTCCTCCT |