Canonical Allele Identifier: CA2186513741

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811806C= , CM000677.2:g.71811806C=	GRCh38
NC_000015.9:g.72104146C= , CM000677.1:g.72104146C=	GRCh37
NC_000015.8:g.69891200C=	NCBI36
NG_009113.2:g.6252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.286C= MANE Select	ENSP00000482504.1:p.His96=
ENST00000617575.4:c.286C=	ENSP00000482504.1:p.His96=
ENST00000621098.1:c.286C=	ENSP00000479962.1:p.His96=
ENST00000621736.4:c.22C=	ENSP00000479254.1:p.His8=
NM_014249.3:c.286C=	NP_055064.1:p.His96=
NM_016346.3:c.286C=	NP_057430.1:p.His96=
XM_011521146.1:c.22C=	XP_011519448.1:p.His8=
NM_014249.4:c.286C= MANE Select	NP_055064.1:p.His96=
NM_016346.4:c.286C=	NP_057430.1:p.His96=