Canonical Allele Identifier:
CA217253338
Gene:
MyVariant.info:
GRCh38
chr11:g.6303404G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6303404G>T , CM000673.2:g.6303404G>T | GRCh38 |
| NC_000011.9:g.6324634G>T , CM000673.1:g.6324634G>T | GRCh37 |
| NC_000011.8:g.6281210G>T | NCBI36 |