Linked Data
dbSNP Id:
rs1656618079
gnomAD v4:
1-218345181-C-T
MyVariant Identifiers:
chr1:g.218518523C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218345181C>T , CM000663.2:g.218345181C>T | GRCh38 |
| NC_000001.10:g.218518523C>T , CM000663.1:g.218518523C>T | GRCh37 |
| NC_000001.9:g.216585146C>T | NCBI36 |
| NG_027721.1:g.4848C>T | |
| NG_027721.2:g.4848C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046268.1:n.284G>A |