Canonical Allele Identifier: CA807794332

Gene: NSG2

Linked Data

• dbSNP Id: rs1324665779
• gnomAD v3: 5-174221173-C-A
• gnomAD v4: 5-174221173-C-A
• MyVariant Identifiers: chr5:g.173648176C>A (hg19) ; chr5:g.174221173C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221173C>A , CM000667.2:g.174221173C>A	GRCh38
NC_000005.9:g.173648176C>A , CM000667.1:g.173648176C>A	GRCh37
NC_000005.8:g.173580782C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+15869C>A	ENSP00000429863.1:n.*18+15869C>A