Canonical Allele Identifier: CA132640536

Gene: NSG2

Linked Data

• dbSNP Id: rs1043295802
• MyVariant Identifiers: chr5:g.173648353G>A (hg19) ; chr5:g.174221350G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221350G>A , CM000667.2:g.174221350G>A	GRCh38
NC_000005.9:g.173648353G>A , CM000667.1:g.173648353G>A	GRCh37
NC_000005.8:g.173580959G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16046G>A	ENSP00000429863.1:n.*18+16046G>A