HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63971997_63971998insTAT , CM000679.2:g.63971997_63971998insTAT | GRCh38 |
NC_000017.10:g.62049357_62049358insTAT , CM000679.1:g.62049357_62049358insTAT | GRCh37 |
NC_000017.9:g.59403089_59403090insTAT | NCBI36 |
NG_011699.1:g.5921_5922insATA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435607.3:c.482+138_482+139insATA MANE Select | ENSP00000396320.1:n.482+138_482+139insATA | |
ENST00000578147.5:c.482+138_482+139insATA | ENSP00000463963.1:n.482+138_482+139insATA | |
NM_000334.4:c.482+138_482+139insATA MANE Select | NP_000325.4:n.482+138_482+139insATA | |
XM_005257566.3:c.482+138_482+139insATA | XP_005257623.1:n.482+138_482+139insATA |