Canonical Allele Identifier: CA807794614
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1428564130
MyVariant Identifiers: chr5:g.173648684C>A (hg19) chr5:g.174221681C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221681C>A , CM000667.2:g.174221681C>A GRCh38
NC_000005.9:g.173648684C>A , CM000667.1:g.173648684C>A GRCh37
NC_000005.8:g.173581290C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16377C>A ENSP00000429863.1:n.*18+16377C>A
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