Canonical Allele Identifier: CA564839804
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1187134124
gnomAD v2: 5-173648104-G-C
gnomAD v3: 5-174221101-G-C
gnomAD v4: 5-174221101-G-C
MyVariant Identifiers: chr5:g.173648104G>C (hg19) chr5:g.174221101G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221101G>C , CM000667.2:g.174221101G>C GRCh38
NC_000005.9:g.173648104G>C , CM000667.1:g.173648104G>C GRCh37
NC_000005.8:g.173580710G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15797G>C ENSP00000429863.1:n.*18+15797G>C
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