Canonical Allele Identifier: CA661668207

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.130748997A>T , CM000672.2:g.130748997A>T	GRCh38
NC_000010.10:g.132547261A>T , CM000672.1:g.132547261A>T	GRCh37
NC_000010.9:g.132437251A>T	NCBI36