Canonical Allele Identifier: CA393032063
Gene: NR2E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811546T>A , CM000677.2:g.71811546T>A GRCh38
NC_000015.9:g.72103886T>A , CM000677.1:g.72103886T>A GRCh37
NC_000015.8:g.69890940T>A NCBI36
NG_009113.2:g.5992T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.182T>A MANE Select ENSP00000482504.1:p.Ile61Asn
ENST00000617575.4:c.182T>A ENSP00000482504.1:p.Ile61Asn
ENST00000621098.1:c.182T>A ENSP00000479962.1:p.Ile61Asn
ENST00000621736.4:c.-83T>A ENSP00000479254.1:n.-83T>A
NM_014249.3:c.182T>A NP_055064.1:p.Ile61Asn
NM_016346.3:c.182T>A NP_057430.1:p.Ile61Asn
XM_011521146.1:c.-83T>A XP_011519448.1:n.-83T>A
NM_014249.4:c.182T>A MANE Select NP_055064.1:p.Ile61Asn
NM_016346.4:c.182T>A NP_057430.1:p.Ile61Asn