Canonical Allele Identifier: CA1602103265

Gene: NSG2

Linked Data

• dbSNP Id: rs1581293688

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221514G>A , CM000667.2:g.174221514G>A	GRCh38
NC_000005.9:g.173648517G>A , CM000667.1:g.173648517G>A	GRCh37
NC_000005.8:g.173581123G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16210G>A	ENSP00000429863.1:n.*18+16210G>A