Linked Data
dbSNP Id:
rs933144912
gnomAD v3:
9-94167412-G-C
gnomAD v4:
9-94167412-G-C
MyVariant Identifiers:
chr9:g.94167412G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.94167412G>C , CM000671.2:g.94167412G>C | GRCh38 |
| NC_000009.11:g.96929694G>C , CM000671.1:g.96929694G>C | GRCh37 |
| NC_000009.10:g.95969515G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_170274.1:n.124+1031G>C | ||
| NR_170275.1:n.124+1031G>C | ||
| NR_170276.1:n.124+1031G>C | ||
| NR_170277.1:n.124+1031G>C | ||
| NR_170278.1:n.124+1031G>C |