Canonical Allele Identifier: CA1602103219
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221442T= , CM000667.2:g.174221442T= GRCh38
NC_000005.9:g.173648445T= , CM000667.1:g.173648445T= GRCh37
NC_000005.8:g.173581051T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16138T= ENSP00000429863.1:n.*18+16138T=