HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63944631_63944632delinsGC , CM000679.2:g.63944631_63944632delinsGC | GRCh38 |
NC_000017.10:g.62021991_62021992delinsGC , CM000679.1:g.62021991_62021992delinsGC | GRCh37 |
NC_000017.9:g.59375723_59375724delinsGC | NCBI36 |
NG_011699.1:g.33287_33288delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435607.3:c.3912+41_3912+42delinsGC MANE Select | ENSP00000396320.1:n.3912+41_3912+42delinsGC | |
ENST00000578147.5:c.3916+37_3916+38delinsGC | ENSP00000463963.1:n.3916+37_3916+38delinsGC | |
NM_000334.4:c.3912+41_3912+42delinsGC MANE Select | NP_000325.4:n.3912+41_3912+42delinsGC | |
XM_005257566.3:c.3912+41_3912+42delinsGC | XP_005257623.1:n.3912+41_3912+42delinsGC |