Canonical Allele Identifier: CA2186513479
Gene: NR2E3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811387T= , CM000677.2:g.71811387T= GRCh38
NC_000015.9:g.72103727T= , CM000677.1:g.72103727T= GRCh37
NC_000015.8:g.69890781T= NCBI36
NG_009113.2:g.5833T=

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.119-96T= MANE Select ENSP00000482504.1:n.119-96T=
ENST00000617575.4:c.119-96T= ENSP00000482504.1:n.119-96T=
ENST00000621098.1:c.119-96T= ENSP00000479962.1:n.119-96T=
ENST00000621736.4:c.-146-96T= ENSP00000479254.1:n.-146-96T=
NM_014249.3:c.119-96T= NP_055064.1:n.119-96T=
NM_016346.3:c.119-96T= NP_057430.1:n.119-96T=
XM_011521146.1:c.-146-96T= XP_011519448.1:n.-146-96T=
NM_014249.4:c.119-96T= MANE Select NP_055064.1:n.119-96T=
NM_016346.4:c.119-96T= NP_057430.1:n.119-96T=