Canonical Allele Identifier:
CA42602845
Gene:
Linked Data
dbSNP Id:
rs970665776
gnomAD v3:
2-11897205-G-T
gnomAD v4:
2-11897205-G-T
MyVariant Identifiers:
chr2:g.11897205G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.11897205G>T , CM000664.2:g.11897205G>T | GRCh38 |
| NC_000002.11:g.12037331G>T , CM000664.1:g.12037331G>T | GRCh37 |
| NC_000002.10:g.11954782G>T | NCBI36 |