Canonical Allele Identifier: CA1084574599
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755680292
gnomAD v3: 5-174221486-C-T
gnomAD v4: 5-174221486-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221486C>T , CM000667.2:g.174221486C>T GRCh38
NC_000005.9:g.173648489C>T , CM000667.1:g.173648489C>T GRCh37
NC_000005.8:g.173581095C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16182C>T ENSP00000429863.1:n.*18+16182C>T
Search 100 bp 5'
Search 100 bp 3'