Canonical Allele Identifier: CA132640531

Gene: NSG2

Linked Data

• dbSNP Id: rs987648330
• MyVariant Identifiers: chr5:g.173648342C>T (hg19) ; chr5:g.174221339C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221339C>T , CM000667.2:g.174221339C>T	GRCh38
NC_000005.9:g.173648342C>T , CM000667.1:g.173648342C>T	GRCh37
NC_000005.8:g.173580948C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16035C>T	ENSP00000429863.1:n.*18+16035C>T