Linked Data
dbSNP Id:
rs1665875011
gnomAD v4:
1-186681191-G-A
MyVariant Identifiers:
chr1:g.186650323G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186681191G>A , CM000663.2:g.186681191G>A | GRCh38 |
| NC_000001.10:g.186650323G>A , CM000663.1:g.186650323G>A | GRCh37 |
| NC_000001.9:g.184916946G>A | NCBI36 |
| NG_028206.2:g.4237C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125801.1:n.538G>A |