Linked Data
dbSNP Id:
rs1218956750
gnomAD v3:
11-62855666-C-T
gnomAD v4:
11-62855666-C-T
MyVariant Identifiers:
chr11:g.62623138C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.62855666C>T , CM000673.2:g.62855666C>T | GRCh38 |
| NC_000011.9:g.62623138C>T , CM000673.1:g.62623138C>T | GRCh37 |
| NC_000011.8:g.62379714C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003098.1:n.25-200G>A | ||
| NR_003098.2:n.22-200G>A | ||
| NR_152575.1:n.220G>A | ||
| NR_152576.1:n.220G>A | ||
| NR_152577.1:n.22-200G>A | ||
| NR_152578.1:n.21+199G>A | ||
| NR_152579.1:n.22-200G>A | ||
| NR_152580.1:n.22-200G>A | ||
| NR_152581.1:n.22-200G>A | ||
| NR_152582.1:n.21+199G>A | ||
| NR_152583.1:n.22-200G>A | ||
| NR_152584.1:n.220G>A | ||
| NR_152585.1:n.220G>A |