Canonical Allele Identifier: CA890203322

Gene:

Linked Data

• dbSNP Id: rs1433880297
• MyVariant Identifiers: chr1:g.161500160T>C (hg19) ; chr1:g.161530370T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161530370T>C , CM000663.2:g.161530370T>C	GRCh38
NC_000001.10:g.161500160T>C , CM000663.1:g.161500160T>C	GRCh37
NC_000001.9:g.159766784T>C	NCBI36