Canonical Allele Identifier: CA564839881
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1283386437
gnomAD v2: 5-173648672-A-G
gnomAD v3: 5-174221669-A-G
gnomAD v4: 5-174221669-A-G
MyVariant Identifiers: chr5:g.173648672A>G (hg19) chr5:g.174221669A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221669A>G , CM000667.2:g.174221669A>G GRCh38
NC_000005.9:g.173648672A>G , CM000667.1:g.173648672A>G GRCh37
NC_000005.8:g.173581278A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16365A>G ENSP00000429863.1:n.*18+16365A>G
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