Canonical Allele Identifier: CA788748206

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147401235A>T , CM000666.2:g.147401235A>T	GRCh38
NC_000004.11:g.148322387A>T , CM000666.1:g.148322387A>T	GRCh37
NC_000004.10:g.148541837A>T	NCBI36