Canonical Allele Identifier: CA2186513649
Gene: NR2E3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811635G= , CM000677.2:g.71811635G= GRCh38
NC_000015.9:g.72103975G= , CM000677.1:g.72103975G= GRCh37
NC_000015.8:g.69891029G= NCBI36
NG_009113.2:g.6081G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.245+26G= MANE Select ENSP00000482504.1:n.245+26G=
ENST00000617575.4:c.245+26G= ENSP00000482504.1:n.245+26G=
ENST00000621098.1:c.245+26G= ENSP00000479962.1:n.245+26G=
ENST00000621736.4:c.-20+26G= ENSP00000479254.1:n.-20+26G=
NM_014249.3:c.245+26G= NP_055064.1:n.245+26G=
NM_016346.3:c.245+26G= NP_057430.1:n.245+26G=
XM_011521146.1:c.-20+26G= XP_011519448.1:n.-20+26G=
NM_014249.4:c.245+26G= MANE Select NP_055064.1:n.245+26G=
NM_016346.4:c.245+26G= NP_057430.1:n.245+26G=
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