Canonical Allele Identifier: CA132640569

Gene: NSG2

Linked Data

• dbSNP Id: rs940818590
• MyVariant Identifiers: chr5:g.173648711T>C (hg19) ; chr5:g.174221708T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221708T>C , CM000667.2:g.174221708T>C	GRCh38
NC_000005.9:g.173648711T>C , CM000667.1:g.173648711T>C	GRCh37
NC_000005.8:g.173581317T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16404T>C	ENSP00000429863.1:n.*18+16404T>C