Canonical Allele Identifier: CA1602103259
Gene: NSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221507_174221510delinsCGTT , CM000667.2:g.174221507_174221510delinsCGTT GRCh38
NC_000005.9:g.173648510_173648513delinsCGTT , CM000667.1:g.173648510_173648513delinsCGTT GRCh37
NC_000005.8:g.173581116_173581119delinsCGTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16203_*18+16206delinsCGTT ENSP00000429863.1:n.*18+16203_*18+16206delinsCGTT
Search 100 bp 5'
Search 100 bp 3'