Canonical Allele Identifier: CA807794523
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1410806862
gnomAD v3: 5-174221553-T-C
gnomAD v4: 5-174221553-T-C
MyVariant Identifiers: chr5:g.173648556T>C (hg19) chr5:g.174221553T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221553T>C , CM000667.2:g.174221553T>C GRCh38
NC_000005.9:g.173648556T>C , CM000667.1:g.173648556T>C GRCh37
NC_000005.8:g.173581162T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16249T>C ENSP00000429863.1:n.*18+16249T>C
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