Canonical Allele Identifier: CA807794634

Gene: NSG2

Linked Data

• dbSNP Id: rs1263460834
• gnomAD v3: 5-174221698-CCT-C
• gnomAD v4: 5-174221698-CCT-C
• MyVariant Identifiers: chr5:g.173648702_173648703del (hg19) ; chr5:g.174221699_174221700del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221699_174221700del , CM000667.2:g.174221699_174221700del	GRCh38
NC_000005.9:g.173648702_173648703del , CM000667.1:g.173648702_173648703del	GRCh37
NC_000005.8:g.173581308_173581309del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16395_*18+16396del	ENSP00000429863.1:n.*18+16395_*18+16396del