Canonical Allele Identifier: CA1602103371
Gene: NSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221742_174221744delinsACT , CM000667.2:g.174221742_174221744delinsACT GRCh38
NC_000005.9:g.173648745_173648747delinsACT , CM000667.1:g.173648745_173648747delinsACT GRCh37
NC_000005.8:g.173581351_173581353delinsACT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16438_*18+16440delinsACT ENSP00000429863.1:n.*18+16438_*18+16440delinsACT
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