Canonical Allele Identifier: CA564831650

Gene: NSG2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174198151T>A , CM000667.2:g.174198151T>A	GRCh38
NC_000005.9:g.173625154T>A , CM000667.1:g.173625154T>A	GRCh37
NC_000005.8:g.173557760T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.214-7049T>A	ENSP00000429863.1:n.214-7049T>A