Canonical Allele Identifier: CA697439499

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33066938A>T , CM000675.2:g.33066938A>T	GRCh38
NC_000013.10:g.33641075A>T , CM000675.1:g.33641075A>T	GRCh37
NC_000013.9:g.32539075A>T	NCBI36
NG_011485.1:g.55505A>T