Canonical Allele Identifier: CA36908862

Gene:

Linked Data

• dbSNP Id: rs747156926
• MyVariant Identifiers: chr1:g.208757140A>G (hg19) ; chr1:g.208583795A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.208583795A>G , CM000663.2:g.208583795A>G	GRCh38
NC_000001.10:g.208757140A>G , CM000663.1:g.208757140A>G	GRCh37
NC_000001.9:g.206823763A>G	NCBI36