Canonical Allele Identifier: CA564839884
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1223428691
gnomAD v2: 5-173648699-C-T
gnomAD v3: 5-174221696-C-T
gnomAD v4: 5-174221696-C-T
MyVariant Identifiers: chr5:g.173648699C>T (hg19) chr5:g.174221696C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221696C>T , CM000667.2:g.174221696C>T GRCh38
NC_000005.9:g.173648699C>T , CM000667.1:g.173648699C>T GRCh37
NC_000005.8:g.173581305C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16392C>T ENSP00000429863.1:n.*18+16392C>T
Search 100 bp 5'
Search 100 bp 3'