Canonical Allele Identifier: CA2769486102
Gene: NSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221186G>A , CM000667.2:g.174221186G>A GRCh38
NC_000005.9:g.173648189G>A , CM000667.1:g.173648189G>A GRCh37
NC_000005.8:g.173580795G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15882G>A ENSP00000429863.1:n.*18+15882G>A
Search 100 bp 5'
Search 100 bp 3'