Canonical Allele Identifier: CA787870052

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.137866906A>T , CM000666.2:g.137866906A>T	GRCh38
NC_000004.11:g.138788060A>T , CM000666.1:g.138788060A>T	GRCh37
NC_000004.10:g.139007510A>T	NCBI36