Canonical Allele Identifier: CA150776648

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156547814G>T , CM000668.2:g.156547814G>T	GRCh38
NC_000006.11:g.156868948G>T , CM000668.1:g.156868948G>T	GRCh37
NC_000006.10:g.156910640G>T	NCBI36