Canonical Allele Identifier: CA14152735
Gene: NR2F2 HGNC NCBI
COSMIC:
COSN25187109 (not active)
MyVariant.info:
GRCh38 chr15:g.96327588A>G
GRCh37 chr15:g.96870817A>G
gnomAD v2:
15:96870817 A / G
gnomAD v3:
15:96327588 A / G
gnomAD v4:
chr15-96327588-A-G
Joint Max Group AF 0.48754542 (EAS)
Genomes Max Group AF 0.48754542 (EAS)
dbSNP:
3743462
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96327588A>G , CM000677.2:g.96327588A>G GRCh38
NC_000015.9:g.96870817A>G , CM000677.1:g.96870817A>G GRCh37
NC_000015.8:g.94671821A>G NCBI36
NG_016753.1:g.6661A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000421109.6:c.43+1236A>G ENSP00000401674.2:n.43+1236A>G
NM_001145155.1:c.43+1236A>G NP_001138627.1:n.43+1236A>G
NM_001145155.2:c.43+1236A>G NP_001138627.1:n.43+1236A>G
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