Canonical Allele Identifier: CA890241539

Gene:

Linked Data

• dbSNP Id: rs1190296351
• MyVariant Identifiers: chr1:g.162030443T>C (hg19) ; chr1:g.162060653T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162060653T>C , CM000663.2:g.162060653T>C	GRCh38
NC_000001.10:g.162030443T>C , CM000663.1:g.162030443T>C	GRCh37
NC_000001.9:g.160297067T>C	NCBI36