Linked Data
MyVariant Identifiers:
chr8:g.129075690_129075691insAGCT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.128063444_128063445insAGCT , CM000670.2:g.128063444_128063445insAGCT | GRCh38 |
| NC_000008.10:g.129075690_129075691insAGCT , CM000670.1:g.129075690_129075691insAGCT | GRCh37 |
| NC_000008.9:g.129144872_129144873insAGCT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003367.3:n.1213-6716_1213-6715insAGCT |