Canonical Allele Identifier: CA770819261

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60307064G>A , CM000664.2:g.60307064G>A	GRCh38
NC_000002.11:g.60534199G>A , CM000664.1:g.60534199G>A	GRCh37
NC_000002.10:g.60387703G>A	NCBI36