Canonical Allele Identifier: CA11187583
Gene: NONOP2 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.60937196G>A
GRCh37 chr2:g.61164331G>A
gnomAD v2:
2:61164331 G / A
gnomAD v3:
2:60937196 G / A
gnomAD v4:
chr2-60937196-G-A
Joint Max Group AF 0.35466145 (NFE)
Genomes Max Group AF 0.36047171 (NFE)
Exomes Max Group AF 0.34903257 (NFE)
dbSNP:
13017599
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.60937196G>A , CM000664.2:g.60937196G>A GRCh38
NC_000002.11:g.61164331G>A , CM000664.1:g.61164331G>A GRCh37
NC_000002.10:g.61017835G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000414613.1:n.854C>T
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