Canonical Allele Identifier:
CA46419067
Gene:
MyVariant.info:
GRCh38
chr2:g.43623451T>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43623451T>A , CM000664.2:g.43623451T>A | GRCh38 |
| NC_000002.11:g.43850590T>A , CM000664.1:g.43850590T>A | GRCh37 |
| NC_000002.10:g.43704094T>A | NCBI36 |