Canonical Allele Identifier: CA202098450

Gene:

Linked Data

• dbSNP Id: rs1003734300
• MyVariant Identifiers: chr10:g.4151135T>A (hg19) ; chr10:g.4108943T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4108943T>A , CM000672.2:g.4108943T>A	GRCh38
NC_000010.10:g.4151135T>A , CM000672.1:g.4151135T>A	GRCh37
NC_000010.9:g.4141135T>A	NCBI36