Canonical Allele Identifier: CA1602103179

Gene: NSG2

Linked Data

• dbSNP Id: rs1755678949

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221365G>A , CM000667.2:g.174221365G>A	GRCh38
NC_000005.9:g.173648368G>A , CM000667.1:g.173648368G>A	GRCh37
NC_000005.8:g.173580974G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16061G>A	ENSP00000429863.1:n.*18+16061G>A