Canonical Allele Identifier: CA51719012

Gene:

Linked Data

• dbSNP Id: rs972761775
• MyVariant Identifiers: chr2:g.85478702T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85478702T>C , CM000664.2:g.85478702T>C	GRCh38
NC_000002.11:g.85705825T>C , CM000664.1:g.85705825T>C	GRCh37
NC_000002.10:g.85559336T>C	NCBI36