Canonical Allele Identifier: CA786414658

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122589917C>G , CM000666.2:g.122589917C>G	GRCh38
NC_000004.11:g.123511072C>G , CM000666.1:g.123511072C>G	GRCh37
NC_000004.10:g.123730522C>G	NCBI36