Canonical Allele Identifier: CA774763028

Gene:

Linked Data

• dbSNP Id: rs190004856
• MyVariant Identifiers: chr17:g.69949097A>G (hg19) ; chr17:g.71952956A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71952956A>G , CM000679.2:g.71952956A>G	GRCh38
NC_000017.10:g.69949097A>G , CM000679.1:g.69949097A>G	GRCh37
NC_000017.9:g.67460692A>G	NCBI36