Canonical Allele Identifier: CA132640552

Gene: NSG2

Linked Data

• dbSNP Id: rs987196796
• MyVariant Identifiers: chr5:g.173648512T>C (hg19) ; chr5:g.174221509T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221509T>C , CM000667.2:g.174221509T>C	GRCh38
NC_000005.9:g.173648512T>C , CM000667.1:g.173648512T>C	GRCh37
NC_000005.8:g.173581118T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000521585.5:c.*18+16205T>C	ENSP00000429863.1:n.*18+16205T>C