Linked Data
dbSNP Id:
rs1382438921
gnomAD v3:
6-31463593-T-TGGTC
gnomAD v4:
6-31463593-T-TGGTC
MyVariant Identifiers:
chr6:g.31431370_31431371insGGTC (hg19)
chr6:g.31463593_31463594insGGTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31463594_31463597dup , CM000668.2:g.31463594_31463597dup | GRCh38 |
| NC_000006.11:g.31431371_31431374dup , CM000668.1:g.31431371_31431374dup | GRCh37 |
| NC_000006.10:g.31539350_31539353dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040662.1:n.324_327dup |