Canonical Allele Identifier: CA1602103283
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221546_174221549delinsCTTT , CM000667.2:g.174221546_174221549delinsCTTT GRCh38
NC_000005.9:g.173648549_173648552delinsCTTT , CM000667.1:g.173648549_173648552delinsCTTT GRCh37
NC_000005.8:g.173581155_173581158delinsCTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16242_*18+16245delinsCTTT ENSP00000429863.1:n.*18+16242_*18+16245delinsCTTT