Canonical Allele Identifier:
CA496057090
Gene:
MyVariant.info:
GRCh37
chr16:g.65895364A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.65861461A>T , CM000678.2:g.65861461A>T | GRCh38 |
| NC_000016.9:g.65895364A>T , CM000678.1:g.65895364A>T | GRCh37 |
| NC_000016.8:g.64452865A>T | NCBI36 |