Canonical Allele Identifier: CA807794328
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1216580347
gnomAD v3: 5-174221151-G-A
gnomAD v4: 5-174221151-G-A
MyVariant Identifiers: chr5:g.173648154G>A (hg19) chr5:g.174221151G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221151G>A , CM000667.2:g.174221151G>A GRCh38
NC_000005.9:g.173648154G>A , CM000667.1:g.173648154G>A GRCh37
NC_000005.8:g.173580760G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15847G>A ENSP00000429863.1:n.*18+15847G>A
Search 100 bp 5'
Search 100 bp 3'