Canonical Allele Identifier: CA1602103366
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs756680032

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221729C>G , CM000667.2:g.174221729C>G GRCh38
NC_000005.9:g.173648732C>G , CM000667.1:g.173648732C>G GRCh37
NC_000005.8:g.173581338C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16425C>G ENSP00000429863.1:n.*18+16425C>G