Linked Data
dbSNP Id:
rs768711182
gnomAD v3:
6-32634232-C-CAAAAAAAAAAAAA
gnomAD v4:
6-32634232-C-CAAAAAAAAAAAAA
MyVariant Identifiers:
chr6:g.32602009_32602010insAAAAAAAAAAAAA (hg19)
chr6:g.32634232_32634233insAAAAAAAAAAAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32634239_32634240insAAAAAAAAAAAAA , CM000668.2:g.32634239_32634240insAAAAAAAAAAAAA | GRCh38 |
| NC_000006.11:g.32602016_32602017insAAAAAAAAAAAAA , CM000668.1:g.32602016_32602017insAAAAAAAAAAAAA | GRCh37 |
| NC_000006.10:g.32709994_32709995insAAAAAAAAAAAAA | NCBI36 |
| NG_032876.1:g.1834_1835insAAAAAAAAAAAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000422863.1:c.-39+1330_-39+1331insAAAAAAAAAAAAA | ENSP00000405797.1:n.-39+1330_-39+1331insAAAAAAAAAAAAA |