Linked Data
dbSNP Id:
rs9357065
gnomAD v2:
6-28129580-T-C
gnomAD v3:
6-28161802-T-C
gnomAD v4:
6-28161802-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.28161802T>C , CM000668.2:g.28161802T>C | GRCh38 |
| NC_000006.11:g.28129580T>C , CM000668.1:g.28129580T>C | GRCh37 |
| NC_000006.10:g.28237559T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562227.2:n.34T>C | ||
| ENST00000440790.6:n.22T>C | ||
| ENST00000570126.1:n.11T>C | ||
| NR_103448.1:n.42T>C |