Canonical Allele Identifier: CA763547494

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203706103G>C , CM000664.2:g.203706103G>C	GRCh38
NC_000002.11:g.204570826G>C , CM000664.1:g.204570826G>C	GRCh37
NC_000002.10:g.204279071G>C	NCBI36
NG_029618.1:g.4629G>C