Canonical Allele Identifier: CA1564182817

Gene: NR2F1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585301C= , CM000667.2:g.93585301C=	GRCh38
NC_000005.9:g.92921007C= , CM000667.1:g.92921007C=	GRCh37
NC_000005.8:g.92946763C=	NCBI36
NG_034119.1:g.6965C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.203C=	ENSP00000481517.1:p.Ser68=
ENST00000327111.8:c.278C= MANE Select	ENSP00000325819.3:p.Ser93=
ENST00000647447.1:c.125C=	ENSP00000495740.1:p.Ser42=
ENST00000327111.7:c.278C=	ENSP00000325819.3:p.Ser93=
ENST00000615873.1:c.203C=	ENSP00000481517.1:p.Ser68=
NM_005654.5:c.278C=	NP_005645.1:p.Ser93=
NM_005654.6:c.278C= MANE Select	NP_005645.1:p.Ser93=