Canonical Allele Identifier: CA1564182848

Gene: NR2F1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585390C= , CM000667.2:g.93585390C=	GRCh38
NC_000005.9:g.92921096C= , CM000667.1:g.92921096C=	GRCh37
NC_000005.8:g.92946852C=	NCBI36
NG_034119.1:g.7054C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.292C=	ENSP00000481517.1:p.Arg98=
ENST00000327111.8:c.367C= MANE Select	ENSP00000325819.3:p.Arg123=
ENST00000647447.1:c.214C=	ENSP00000495740.1:p.Arg72=
ENST00000327111.7:c.367C=	ENSP00000325819.3:p.Arg123=
ENST00000615873.1:c.292C=	ENSP00000481517.1:p.Arg98=
NM_005654.5:c.367C=	NP_005645.1:p.Arg123=
NM_005654.6:c.367C= MANE Select	NP_005645.1:p.Arg123=