Canonical Allele Identifier: CA449368132

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29938914A>T , CM000668.2:g.29938914A>T	GRCh38
NC_000006.11:g.29906691A>T , CM000668.1:g.29906691A>T	GRCh37
NC_000006.10:g.30014670A>T	NCBI36
NG_029217.2:g.1445A>T