Canonical Allele Identifier: CA132640532

Gene: NSG2

Linked Data

• dbSNP Id: rs375602749
• MyVariant Identifiers: chr5:g.173648346_173648347insT (hg19) ; chr5:g.174221343_174221344insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221344dup , CM000667.2:g.174221344dup	GRCh38
NC_000005.9:g.173648347dup , CM000667.1:g.173648347dup	GRCh37
NC_000005.8:g.173580953dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16040dup	ENSP00000429863.1:n.*18+16040dup