Canonical Allele Identifier: CA807794593
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1467321051
gnomAD v3: 5-174221658-TA-T
gnomAD v4: 5-174221658-TA-T
MyVariant Identifiers: chr5:g.173648662del (hg19) chr5:g.174221659del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221660del , CM000667.2:g.174221660del GRCh38
NC_000005.9:g.173648663del , CM000667.1:g.173648663del GRCh37
NC_000005.8:g.173581269del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16356del ENSP00000429863.1:n.*18+16356del
Search 100 bp 5'
Search 100 bp 3'