Canonical Allele Identifier: CA2710513738
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2113100267

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221063T>A , CM000667.2:g.174221063T>A GRCh38
NC_000005.9:g.173648066T>A , CM000667.1:g.173648066T>A GRCh37
NC_000005.8:g.173580672T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15759T>A ENSP00000429863.1:n.*18+15759T>A