Canonical Allele Identifier: CA7750646
Gene: NR2F2 HGNC NCBI
NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs751185533
ExAC: 15:96869606 C / T
gnomAD v2: 15-96869606-C-T
gnomAD v3: 15-96326377-C-T
gnomAD v4: 15-96326377-C-T
MyVariant Identifiers: chr15:g.96869606C>T (hg19) chr15:g.96326377C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96326377C>T , CM000677.2:g.96326377C>T GRCh38
NC_000015.9:g.96869606C>T , CM000677.1:g.96869606C>T GRCh37
NC_000015.8:g.94670610C>T NCBI36
NG_016753.1:g.5450C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000421109.6:c.43+25C>T (NR2F2) ENSP00000401674.2:n.43+25C>T
NM_001145155.1:c.43+25C>T (NR2F2) NP_001138627.1:n.43+25C>T
NR_102743.1:n.163+822G>A (NR2F2-AS1)
NR_102744.1:n.163+822G>A (NR2F2-AS1)
NR_125738.1:n.163+579G>A (NR2F2-AS1)
NM_001145155.2:c.43+25C>T (NR2F2) NP_001138627.1:n.43+25C>T
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