Canonical Allele Identifier: CA807794666

Gene: NSG2

Linked Data

• dbSNP Id: rs1166652079
• MyVariant Identifiers: chr5:g.173648746_173648747del (hg19) ; chr5:g.174221743_174221744del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221745_174221746del , CM000667.2:g.174221745_174221746del	GRCh38
NC_000005.9:g.173648748_173648749del , CM000667.1:g.173648748_173648749del	GRCh37
NC_000005.8:g.173581354_173581355del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16441_*18+16442del	ENSP00000429863.1:n.*18+16441_*18+16442del