Canonical Allele Identifier: CA7750735

Gene: NR2F2

Linked Data

• ClinVar Variation Id: 477848
• ClinVar RCV Id: RCV000526939
• dbSNP Id: rs143951395
• ExAC: 15:96877399 C / T
• gnomAD v2: 15-96877399-C-T
• gnomAD v3: 15-96334170-C-T
• gnomAD v4: 15-96334170-C-T
• MyVariant Identifiers: chr15:g.96877399C>T (hg19) ; chr15:g.96334170C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96334170C>T , CM000677.2:g.96334170C>T	GRCh38
NC_000015.9:g.96877399C>T , CM000677.1:g.96877399C>T	GRCh37
NC_000015.8:g.94678403C>T	NCBI36
NG_016753.1:g.13243C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394166.8:c.537C>T MANE Select	ENSP00000377721.3:p.Ser179=
ENST00000394166.7:c.537C>T	ENSP00000377721.3:p.Ser179=
ENST00000394171.6:c.78C>T	ENSP00000377726.2:p.Ser26=
ENST00000421109.6:c.138C>T	ENSP00000401674.2:p.Ser46=
ENST00000453270.2:c.78C>T	ENSP00000389853.2:p.Ser26=
ENST00000559679.1:c.78C>T	ENSP00000457112.1:p.Ser26=
NM_001145155.1:c.138C>T	NP_001138627.1:p.Ser46=
NM_001145156.1:c.78C>T	NP_001138628.1:p.Ser26=
NM_001145157.1:c.78C>T	NP_001138629.1:p.Ser26=
NM_021005.3:c.537C>T	NP_066285.1:p.Ser179=
NM_021005.4:c.537C>T MANE Select	NP_066285.1:p.Ser179=
NM_001145155.2:c.138C>T	NP_001138627.1:p.Ser46=
NM_001145157.2:c.78C>T	NP_001138629.1:p.Ser26=