Canonical Allele Identifier: CA1602103350
Gene: NSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221698_174221700delinsCCT , CM000667.2:g.174221698_174221700delinsCCT GRCh38
NC_000005.9:g.173648701_173648703delinsCCT , CM000667.1:g.173648701_173648703delinsCCT GRCh37
NC_000005.8:g.173581307_173581309delinsCCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16394_*18+16396delinsCCT ENSP00000429863.1:n.*18+16394_*18+16396delinsCCT
Search 100 bp 5'
Search 100 bp 3'