Canonical Allele Identifier: CA807794321
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs999035999
gnomAD v3: 5-174221136-T-A
gnomAD v4: 5-174221136-T-A
MyVariant Identifiers: chr5:g.173648139T>A (hg19) chr5:g.174221136T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221136T>A , CM000667.2:g.174221136T>A GRCh38
NC_000005.9:g.173648139T>A , CM000667.1:g.173648139T>A GRCh37
NC_000005.8:g.173580745T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15832T>A ENSP00000429863.1:n.*18+15832T>A
Search 100 bp 5'
Search 100 bp 3'