Canonical Allele Identifier: CA807794449

Gene: NSG2

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221435T>A , CM000667.2:g.174221435T>A	GRCh38
NC_000005.9:g.173648438T>A , CM000667.1:g.173648438T>A	GRCh37
NC_000005.8:g.173581044T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16131T>A	ENSP00000429863.1:n.*18+16131T>A