Canonical Allele Identifier: CA2186513492
Gene: NR2E3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811408G= , CM000677.2:g.71811408G= GRCh38
NC_000015.9:g.72103748G= , CM000677.1:g.72103748G= GRCh37
NC_000015.8:g.69890802G= NCBI36
NG_009113.2:g.5854G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.119-75G= MANE Select ENSP00000482504.1:n.119-75G=
ENST00000617575.4:c.119-75G= ENSP00000482504.1:n.119-75G=
ENST00000621098.1:c.119-75G= ENSP00000479962.1:n.119-75G=
ENST00000621736.4:c.-146-75G= ENSP00000479254.1:n.-146-75G=
NM_014249.3:c.119-75G= NP_055064.1:n.119-75G=
NM_016346.3:c.119-75G= NP_057430.1:n.119-75G=
XM_011521146.1:c.-146-75G= XP_011519448.1:n.-146-75G=
NM_014249.4:c.119-75G= MANE Select NP_055064.1:n.119-75G=
NM_016346.4:c.119-75G= NP_057430.1:n.119-75G=