Canonical Allele Identifier: CA1602103347
Gene: NSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221694_174221695delinsAG , CM000667.2:g.174221694_174221695delinsAG GRCh38
NC_000005.9:g.173648697_173648698delinsAG , CM000667.1:g.173648697_173648698delinsAG GRCh37
NC_000005.8:g.173581303_173581304delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16390_*18+16391delinsAG ENSP00000429863.1:n.*18+16390_*18+16391delinsAG
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