Canonical Allele Identifier: CA882135103

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3944242G>T , CM000681.2:g.3944242G>T	GRCh38
NC_000019.9:g.3944240G>T , CM000681.1:g.3944240G>T	GRCh37
NC_000019.8:g.3895240G>T	NCBI36