Canonical Allele Identifier: CA789377738

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154602694A>G , CM000666.2:g.154602694A>G	GRCh38
NC_000004.11:g.155523846A>G , CM000666.1:g.155523846A>G	GRCh37
NC_000004.10:g.155743296A>G	NCBI36
NG_008834.1:g.15057T>C