Canonical Allele Identifier: CA2555478296
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221145A>G , CM000667.2:g.174221145A>G GRCh38
NC_000005.9:g.173648148A>G , CM000667.1:g.173648148A>G GRCh37
NC_000005.8:g.173580754A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15841A>G ENSP00000429863.1:n.*18+15841A>G