Canonical Allele Identifier: CA885823013

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114697195A>T , CM000663.2:g.114697195A>T	GRCh38
NC_000001.10:g.115239816A>T , CM000663.1:g.115239816A>T	GRCh37
NC_000001.9:g.115041339A>T	NCBI36
NG_008012.1:g.3361T>A