Canonical Allele Identifier: CA1602103363
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221720G= , CM000667.2:g.174221720G= GRCh38
NC_000005.9:g.173648723G= , CM000667.1:g.173648723G= GRCh37
NC_000005.8:g.173581329G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16416G= ENSP00000429863.1:n.*18+16416G=