Canonical Allele Identifier: CA116349020

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.28340063C>T , CM000667.2:g.28340063C>T	GRCh38
NC_000005.9:g.28340170C>T , CM000667.1:g.28340170C>T	GRCh37
NC_000005.8:g.28375927C>T	NCBI36