Linked Data
dbSNP Id:
rs1665877301
gnomAD v4:
1-186681306-C-A
MyVariant Identifiers:
chr1:g.186650438C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186681306C>A , CM000663.2:g.186681306C>A | GRCh38 |
| NC_000001.10:g.186650438C>A , CM000663.1:g.186650438C>A | GRCh37 |
| NC_000001.9:g.184917061C>A | NCBI36 |
| NG_028206.2:g.4122G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125801.1:n.653C>A |