Canonical Allele Identifier: CA803785900

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1308437G>T , CM000667.2:g.1308437G>T	GRCh38
NC_000005.9:g.1308552G>T , CM000667.1:g.1308552G>T	GRCh37
NC_000005.8:g.1361552G>T	NCBI36