Canonical Allele Identifier: CA448291341

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.205920G>A , CM000668.2:g.205920G>A	GRCh38
NC_000006.11:g.205920G>A , CM000668.1:g.205920G>A	GRCh37
NC_000006.10:g.150920G>A	NCBI36