Canonical Allele Identifier: CA2186513622

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811591G= , CM000677.2:g.71811591G=	GRCh38
NC_000015.9:g.72103931G= , CM000677.1:g.72103931G=	GRCh37
NC_000015.8:g.69890985G=	NCBI36
NG_009113.2:g.6037G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.227G= MANE Select	ENSP00000482504.1:p.Arg76=
ENST00000617575.4:c.227G=	ENSP00000482504.1:p.Arg76=
ENST00000621098.1:c.227G=	ENSP00000479962.1:p.Arg76=
ENST00000621736.4:c.-38G=	ENSP00000479254.1:n.-38G=
NM_014249.3:c.227G=	NP_055064.1:p.Arg76=
NM_016346.3:c.227G=	NP_057430.1:p.Arg76=
XM_011521146.1:c.-38G=	XP_011519448.1:n.-38G=
NM_014249.4:c.227G= MANE Select	NP_055064.1:p.Arg76=
NM_016346.4:c.227G=	NP_057430.1:p.Arg76=