HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202376547_202376548insGGCGGCCGCGGC , CM000664.2:g.202376547_202376548insGGCGGCCGCGGC | GRCh38 |
NC_000002.11:g.203241270_203241271insGGCGGCCGCGGC , CM000664.1:g.203241270_203241271insGGCGGCCGCGGC | GRCh37 |
NC_000002.10:g.202949515_202949516insGGCGGCCGCGGC | NCBI36 |
NG_009363.1:g.5221_5222insGGCGGCCGCGGC , LRG_712:g.5221_5222insGGCGGCCGCGGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.-928_-927insGGCGGCCGCGGC MANE Select | ENSP00000363708.4:n.-928_-927insGGCGGCCGCGGC | |
NM_001204.6:c.-928_-927insGGCGGCCGCGGC , LRG_712t1:c.-928_-927insGGCGGCCGCGGC | NP_001195.2:n.-928_-927insGGCGGCCGCGGC | |
XM_011511687.1:c.-928_-927insGGCGGCCGCGGC | XP_011509989.1:n.-928_-927insGGCGGCCGCGGC | |
XM_011511688.1:c.-928_-927insGGCGGCCGCGGC | XP_011509990.1:n.-928_-927insGGCGGCCGCGGC | |
NM_001204.7:c.-928_-927insGGCGGCCGCGGC MANE Select | NP_001195.2:n.-928_-927insGGCGGCCGCGGC |