Canonical Allele Identifier: CA2186513714
Gene: NR2E3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811752C= , CM000677.2:g.71811752C= GRCh38
NC_000015.9:g.72104092C= , CM000677.1:g.72104092C= GRCh37
NC_000015.8:g.69891146C= NCBI36
NG_009113.2:g.6198C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.246-14C= MANE Select ENSP00000482504.1:n.246-14C=
ENST00000617575.4:c.246-14C= ENSP00000482504.1:n.246-14C=
ENST00000621098.1:c.246-14C= ENSP00000479962.1:n.246-14C=
ENST00000621736.4:c.-19-14C= ENSP00000479254.1:n.-19-14C=
NM_014249.3:c.246-14C= NP_055064.1:n.246-14C=
NM_016346.3:c.246-14C= NP_057430.1:n.246-14C=
XM_011521146.1:c.-19-14C= XP_011519448.1:n.-19-14C=
NM_014249.4:c.246-14C= MANE Select NP_055064.1:n.246-14C=
NM_016346.4:c.246-14C= NP_057430.1:n.246-14C=
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