Canonical Allele Identifier: CA877710877

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.69585474A>C , CM000685.2:g.69585474A>C	GRCh38
NC_000023.10:g.68805318A>C , CM000685.1:g.68805318A>C	GRCh37
NC_000023.9:g.68722043A>C	NCBI36