Canonical Allele Identifier: CA705269029

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35405286G>C , CM000676.2:g.35405286G>C	GRCh38
NC_000014.8:g.35874492G>C , CM000676.1:g.35874492G>C	GRCh37
NC_000014.7:g.34944243G>C	NCBI36
NG_007571.1:g.4453C>G , LRG_89:g.4453C>G