Canonical Allele Identifier: CA2606454026
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2113101062
gnomAD v3: 5-174221735-C-T
gnomAD v4: 5-174221735-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221735C>T , CM000667.2:g.174221735C>T GRCh38
NC_000005.9:g.173648738C>T , CM000667.1:g.173648738C>T GRCh37
NC_000005.8:g.173581344C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16431C>T ENSP00000429863.1:n.*18+16431C>T
Search 100 bp 5'
Search 100 bp 3'