Canonical Allele Identifier:
CA60483049
Gene:
MyVariant.info:
GRCh38
chr2:g.168286525G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.168286525G>T , CM000664.2:g.168286525G>T | GRCh38 |
| NC_000002.11:g.169143035G>T , CM000664.1:g.169143035G>T | GRCh37 |
| NC_000002.10:g.168851281G>T | NCBI36 |