Linked Data
dbSNP Id:
rs367965026
MyVariant Identifiers:
chr21:g.36673554_36673555insCCTG (hg19)
chr21:g.35301256_35301257insCCTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.35301256_35301257insCCTG , CM000683.2:g.35301256_35301257insCCTG | GRCh38 |
| NC_000021.8:g.36673554_36673555insCCTG , CM000683.1:g.36673554_36673555insCCTG | GRCh37 |
| NC_000021.7:g.35595424_35595425insCCTG | NCBI36 |
| NG_011402.2:g.688454_688455insCAGG , LRG_482:g.688454_688455insCAGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475045.6:c.-197+160704_-197+160705insCAGG | ENSP00000477072.1:n.-197+160704_-197+160705insCAGG |