Canonical Allele Identifier: CA807794564

Gene: NSG2

Linked Data

• dbSNP Id: rs1386257154
• gnomAD v3: 5-174221638-C-G
• gnomAD v4: 5-174221638-C-G
• MyVariant Identifiers: chr5:g.173648641C>G (hg19) ; chr5:g.174221638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221638C>G , CM000667.2:g.174221638C>G	GRCh38
NC_000005.9:g.173648641C>G , CM000667.1:g.173648641C>G	GRCh37
NC_000005.8:g.173581247C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16334C>G	ENSP00000429863.1:n.*18+16334C>G