Canonical Allele Identifier: CA10603492
Gene: NR2F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 280543
ClinVar RCV Id: RCV000384214 RCV001171515
dbSNP Id: rs886041730
MyVariant Identifiers: chr15:g.96877718dupG (hg19) chr15:g.96334489dupG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96334489dup , CM000677.2:g.96334489dup GRCh38
NC_000015.9:g.96877718dup , CM000677.1:g.96877718dup GRCh37
NC_000015.8:g.94678722dup NCBI36
NG_016753.1:g.13562dup

Transcript Alleles

HGVS Amino-acid change
ENST00000394166.8:c.856dup MANE Select ENSP00000377721.3:p.Val286GlyfsTer23
ENST00000394166.7:c.856dup ENSP00000377721.3:p.Val286GlyfsTer23
ENST00000394171.6:c.397dup ENSP00000377726.2:p.Val133GlyfsTer23
ENST00000421109.6:c.457dup ENSP00000401674.2:p.Val153GlyfsTer23
ENST00000453270.2:c.397dup ENSP00000389853.2:p.Val133GlyfsTer23
NM_001145155.1:c.457dup NP_001138627.1:p.Val153GlyfsTer23
NM_001145156.1:c.397dup NP_001138628.1:p.Val133GlyfsTer23
NM_001145157.1:c.397dup NP_001138629.1:p.Val133GlyfsTer23
NM_021005.3:c.856dup NP_066285.1:p.Val286GlyfsTer23
NM_021005.4:c.856dup MANE Select NP_066285.1:p.Val286GlyfsTer23
NM_001145155.2:c.457dup NP_001138627.1:p.Val153GlyfsTer23
NM_001145157.2:c.397dup NP_001138629.1:p.Val133GlyfsTer23
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