Canonical Allele Identifier: CA789427239

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155134181C>T , CM000666.2:g.155134181C>T	GRCh38
NC_000004.11:g.156055333C>T , CM000666.1:g.156055333C>T	GRCh37
NC_000004.10:g.156274783C>T	NCBI36