Canonical Allele Identifier: CA2606454023
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755679117
gnomAD v3: 5-174221378-A-G
gnomAD v4: 5-174221378-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221378A>G , CM000667.2:g.174221378A>G GRCh38
NC_000005.9:g.173648381A>G , CM000667.1:g.173648381A>G GRCh37
NC_000005.8:g.173580987A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16074A>G ENSP00000429863.1:n.*18+16074A>G
Search 100 bp 5'
Search 100 bp 3'