Canonical Allele Identifier: CA2186513703
Gene: NR2E3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811738A= , CM000677.2:g.71811738A= GRCh38
NC_000015.9:g.72104078A= , CM000677.1:g.72104078A= GRCh37
NC_000015.8:g.69891132A= NCBI36
NG_009113.2:g.6184A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.246-28A= MANE Select ENSP00000482504.1:n.246-28A=
ENST00000617575.4:c.246-28A= ENSP00000482504.1:n.246-28A=
ENST00000621098.1:c.246-28A= ENSP00000479962.1:n.246-28A=
ENST00000621736.4:c.-19-28A= ENSP00000479254.1:n.-19-28A=
NM_014249.3:c.246-28A= NP_055064.1:n.246-28A=
NM_016346.3:c.246-28A= NP_057430.1:n.246-28A=
XM_011521146.1:c.-19-28A= XP_011519448.1:n.-19-28A=
NM_014249.4:c.246-28A= MANE Select NP_055064.1:n.246-28A=
NM_016346.4:c.246-28A= NP_057430.1:n.246-28A=
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