Canonical Allele Identifier: CA1602103200
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221395G= , CM000667.2:g.174221395G= GRCh38
NC_000005.9:g.173648398G= , CM000667.1:g.173648398G= GRCh37
NC_000005.8:g.173581004G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16091G= ENSP00000429863.1:n.*18+16091G=