Canonical Allele Identifier: CA300346752
Gene:

Linked Data

dbSNP Id: rs962219609
MyVariant Identifiers: chr18:g.49001512G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49001512G>C , CM000680.2:g.49001512G>C GRCh38
NC_000018.9:g.46527882G>C , CM000680.1:g.46527882G>C GRCh37
NC_000018.8:g.44781880G>C NCBI36