Canonical Allele Identifier: CA132640509
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1012286888
MyVariant Identifiers: chr5:g.174221198A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221198A>G , CM000667.2:g.174221198A>G GRCh38
NC_000005.9:g.173648201A>G , CM000667.1:g.173648201A>G GRCh37
NC_000005.8:g.173580807A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15894A>G ENSP00000429863.1:n.*18+15894A>G