Canonical Allele Identifier: CA1602103338
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221682T= , CM000667.2:g.174221682T= GRCh38
NC_000005.9:g.173648685T= , CM000667.1:g.173648685T= GRCh37
NC_000005.8:g.173581291T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16378T= ENSP00000429863.1:n.*18+16378T=