Canonical Allele Identifier: CA132640540
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1052680466
MyVariant Identifiers: chr5:g.173648401C>T (hg19) chr5:g.174221398C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221398C>T , CM000667.2:g.174221398C>T GRCh38
NC_000005.9:g.173648401C>T , CM000667.1:g.173648401C>T GRCh37
NC_000005.8:g.173581007C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16094C>T ENSP00000429863.1:n.*18+16094C>T
Search 100 bp 5'
Search 100 bp 3'