Canonical Allele Identifier: CA1602103341
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755681776
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221686G>T , CM000667.2:g.174221686G>T GRCh38
NC_000005.9:g.173648689G>T , CM000667.1:g.173648689G>T GRCh37
NC_000005.8:g.173581295G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16382G>T ENSP00000429863.1:n.*18+16382G>T
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