Canonical Allele Identifier: CA807794479

Gene: NSG2

Linked Data

• dbSNP Id: rs1287932604
• gnomAD v3: 5-174221516-T-TA
• gnomAD v4: 5-174221516-T-TA
• MyVariant Identifiers: chr5:g.173648519_173648520insA (hg19) ; chr5:g.174221516_174221517insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221518dup , CM000667.2:g.174221518dup	GRCh38
NC_000005.9:g.173648521dup , CM000667.1:g.173648521dup	GRCh37
NC_000005.8:g.173581127dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16214dup	ENSP00000429863.1:n.*18+16214dup