Canonical Allele Identifier: CA27681450

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100718225C>T , CM000663.2:g.100718225C>T	GRCh38
NC_000001.10:g.101183781C>T , CM000663.1:g.101183781C>T	GRCh37
NC_000001.9:g.100956369C>T	NCBI36
NG_023034.2:g.3485C>T