Canonical Allele Identifier: CA1602103051
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221091C= , CM000667.2:g.174221091C= GRCh38
NC_000005.9:g.173648094C= , CM000667.1:g.173648094C= GRCh37
NC_000005.8:g.173580700C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15787C= ENSP00000429863.1:n.*18+15787C=