HGVS | Genome Assembly |
---|---|
NC_000001.11:g.46399224_46399225delinsGC , CM000663.2:g.46399224_46399225delinsGC | GRCh38 |
NC_000001.10:g.46864896_46864897delinsGC , CM000663.1:g.46864896_46864897delinsGC | GRCh37 |
NC_000001.9:g.46637483_46637484delinsGC | NCBI36 |
NG_012195.1:g.9958_9959delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243167.9:c.196-2867_196-2866delinsGC MANE Select | ENSP00000243167.8:n.196-2867_196-2866delinsGC | |
ENST00000243167.8:c.196-2867_196-2866delinsGC | ENSP00000243167.8:n.196-2867_196-2866delinsGC | |
ENST00000468718.5:n.216-2867_216-2866delinsGC | ||
ENST00000493735.5:n.174-2867_174-2866delinsGC | ||
NM_001441.2:c.196-2867_196-2866delinsGC | NP_001432.2:n.196-2867_196-2866delinsGC | |
NM_001441.3:c.196-2867_196-2866delinsGC MANE Select | NP_001432.2:n.196-2867_196-2866delinsGC |