Canonical Allele Identifier: CA1084574628
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755681280
gnomAD v3: 5-174221611-C-G
gnomAD v4: 5-174221611-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221611C>G , CM000667.2:g.174221611C>G GRCh38
NC_000005.9:g.173648614C>G , CM000667.1:g.173648614C>G GRCh37
NC_000005.8:g.173581220C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16307C>G ENSP00000429863.1:n.*18+16307C>G
Search 100 bp 5'
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