Canonical Allele Identifier: CA1602103311
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755681380

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221624_174221630del , CM000667.2:g.174221624_174221630del GRCh38
NC_000005.9:g.173648627_173648633del , CM000667.1:g.173648627_173648633del GRCh37
NC_000005.8:g.173581233_173581239del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16320_*18+16326del ENSP00000429863.1:n.*18+16320_*18+16326del