Canonical Allele Identifier:
CA101676572
Gene:
MyVariant.info:
GRCh38
chr4:g.99353053C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99353053C>T , CM000666.2:g.99353053C>T | GRCh38 |
| NC_000004.11:g.100274210C>T , CM000666.1:g.100274210C>T | GRCh37 |
| NC_000004.10:g.100493233C>T | NCBI36 |
| NG_011718.1:g.4708G>A |