Canonical Allele Identifier:
CA291300966
Gene:
MyVariant.info:
GRCh38
chr17:g.47731462T>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47731462T>A , CM000679.2:g.47731462T>A | GRCh38 |
| NC_000017.10:g.45808828T>A , CM000679.1:g.45808828T>A | GRCh37 |
| NC_000017.9:g.43163827T>A | NCBI36 |
| NG_012166.1:g.3219T>A |