Canonical Allele Identifier: CA2198017565

Gene: NR2F2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96337399C= , CM000677.2:g.96337399C=	GRCh38
NC_000015.9:g.96880628C= , CM000677.1:g.96880628C=	GRCh37
NC_000015.8:g.94681632C=	NCBI36
NG_016753.1:g.16472C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394166.8:c.1022C= MANE Select	ENSP00000377721.3:p.Ser341=
ENST00000394166.7:c.1022C=	ENSP00000377721.3:p.Ser341=
ENST00000394171.6:c.563C=	ENSP00000377726.2:p.Ser188=
ENST00000421109.6:c.623C=	ENSP00000401674.2:p.Ser208=
ENST00000453270.2:c.563C=	ENSP00000389853.2:p.Ser188=
NM_001145155.1:c.623C=	NP_001138627.1:p.Ser208=
NM_001145156.1:c.563C=	NP_001138628.1:p.Ser188=
NM_001145157.1:c.563C=	NP_001138629.1:p.Ser188=
NM_021005.3:c.1022C=	NP_066285.1:p.Ser341=
NM_021005.4:c.1022C= MANE Select	NP_066285.1:p.Ser341=
NM_001145155.2:c.623C=	NP_001138627.1:p.Ser208=
NM_001145157.2:c.563C=	NP_001138629.1:p.Ser188=