Canonical Allele Identifier: CA1602103058
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221114A= , CM000667.2:g.174221114A= GRCh38
NC_000005.9:g.173648117A= , CM000667.1:g.173648117A= GRCh37
NC_000005.8:g.173580723A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15810A= ENSP00000429863.1:n.*18+15810A=