Canonical Allele Identifier: CA1084574572
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755679194

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221388C>A , CM000667.2:g.174221388C>A GRCh38
NC_000005.9:g.173648391C>A , CM000667.1:g.173648391C>A GRCh37
NC_000005.8:g.173580997C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16084C>A ENSP00000429863.1:n.*18+16084C>A