Canonical Allele Identifier: CA2710513739
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2113100286

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221074C>A , CM000667.2:g.174221074C>A GRCh38
NC_000005.9:g.173648077C>A , CM000667.1:g.173648077C>A GRCh37
NC_000005.8:g.173580683C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15770C>A ENSP00000429863.1:n.*18+15770C>A