Canonical Allele Identifier: CA807794651

Gene: NSG2

Linked Data

• dbSNP Id: rs1398133785
• gnomAD v3: 5-174221720-G-T
• gnomAD v4: 5-174221720-G-T
• MyVariant Identifiers: chr5:g.173648723G>T (hg19) ; chr5:g.174221720G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221720G>T , CM000667.2:g.174221720G>T	GRCh38
NC_000005.9:g.173648723G>T , CM000667.1:g.173648723G>T	GRCh37
NC_000005.8:g.173581329G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16416G>T	ENSP00000429863.1:n.*18+16416G>T