Canonical Allele Identifier: CA1602103030
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755676184
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221051G>A , CM000667.2:g.174221051G>A GRCh38
NC_000005.9:g.173648054G>A , CM000667.1:g.173648054G>A GRCh37
NC_000005.8:g.173580660G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15747G>A ENSP00000429863.1:n.*18+15747G>A
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