Canonical Allele Identifier: CA101676594

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99353067C>T , CM000666.2:g.99353067C>T	GRCh38
NC_000004.11:g.100274224C>T , CM000666.1:g.100274224C>T	GRCh37
NC_000004.10:g.100493247C>T	NCBI36
NG_011718.1:g.4694G>A