Canonical Allele Identifier: CA917642881
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1561706002

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221543del , CM000667.2:g.174221543del GRCh38
NC_000005.9:g.173648546del , CM000667.1:g.173648546del GRCh37
NC_000005.8:g.173581152del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16239del ENSP00000429863.1:n.*18+16239del