Canonical Allele Identifier: CA779991202

Gene:

Linked Data

• dbSNP Id: rs1239406321
• gnomAD v3: 18-49001527-G-A
• gnomAD v4: 18-49001527-G-A
• MyVariant Identifiers: chr18:g.46527897G>A (hg19) ; chr18:g.49001527G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49001527G>A , CM000680.2:g.49001527G>A	GRCh38
NC_000018.9:g.46527897G>A , CM000680.1:g.46527897G>A	GRCh37
NC_000018.8:g.44781895G>A	NCBI36