Linked Data
dbSNP Id:
rs2100858709
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418433_94418434insTCCGCCGCCGCC , CM000663.2:g.94418433_94418434insTCCGCCGCCGCC | GRCh38 |
| NC_000001.10:g.94883989_94883990insTCCGCCGCCGCC , CM000663.1:g.94883989_94883990insTCCGCCGCCGCC | GRCh37 |
| NC_000001.9:g.94656577_94656578insTCCGCCGCCGCC | NCBI36 |
| NG_008865.1:g.5057_5058insTCCGCCGCCGCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.-46_-45insTCCGCCGCCGCC MANE Select | ENSP00000359233.4:n.-46_-45insTCCGCCGCCGCC | |
| NM_001122674.1:c.-46_-45insTCCGCCGCCGCC | NP_001116146.1:n.-46_-45insTCCGCCGCCGCC | |
| NM_002858.3:c.-46_-45insTCCGCCGCCGCC | NP_002849.1:n.-46_-45insTCCGCCGCCGCC | |
| XM_006710802.2:c.-46_-45insTCCGCCGCCGCC | XP_006710865.2:n.-46_-45insTCCGCCGCCGCC | |
| NM_002858.4:c.-46_-45insTCCGCCGCCGCC MANE Select | NP_002849.1:n.-46_-45insTCCGCCGCCGCC | |
| NM_001122674.2:c.-46_-45insTCCGCCGCCGCC | NP_001116146.1:n.-46_-45insTCCGCCGCCGCC |