Canonical Allele Identifier:
CA118221482
Gene:
MyVariant.info:
GRCh38
chr5:g.44822356G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.44822356G>T , CM000667.2:g.44822356G>T | GRCh38 |
| NC_000005.9:g.44822458G>T , CM000667.1:g.44822458G>T | GRCh37 |
| NC_000005.8:g.44858215G>T | NCBI36 |