HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67754371_67754376delinsTGGTGC , CM000666.2:g.67754371_67754376delinsTGGTGC | GRCh38 |
NC_000004.11:g.68620089_68620094delinsTGGTGC , CM000666.1:g.68620089_68620094delinsTGGTGC | GRCh37 |
NC_000004.10:g.68302684_68302689delinsTGGTGC | NCBI36 |
NG_009293.1:g.6711_6716delinsGCACCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.-41_-36delinsGCACCA MANE Select | ENSP00000226413.5:n.-41_-36delinsGCACCA | |
NM_000406.2:c.-41_-36delinsGCACCA | NP_000397.1:n.-41_-36delinsGCACCA | |
NM_001012763.1:c.-41_-36delinsGCACCA | NP_001012781.1:n.-41_-36delinsGCACCA | |
NM_000406.3:c.-41_-36delinsGCACCA MANE Select | NP_000397.1:n.-41_-36delinsGCACCA | |
NM_001012763.2:c.-41_-36delinsGCACCA | NP_001012781.1:n.-41_-36delinsGCACCA |