Canonical Allele Identifier: CA2629291537
Gene: NR2E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811481_71811495dup , CM000677.2:g.71811481_71811495dup GRCh38
NC_000015.9:g.72103821_72103835dup , CM000677.1:g.72103821_72103835dup GRCh37
NC_000015.8:g.69890875_69890889dup NCBI36
NG_009113.2:g.5927_5941dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.119-2_131dup
ENST00000617575.4:c.119-2_131dup
ENST00000621098.1:c.119-2_131dup
ENST00000621736.4:c.-146-2_-134dup
NM_014249.3:c.119-2_131dup
NM_016346.3:c.119-2_131dup
XM_011521146.1:c.-146-2_-134dup
NM_014249.4:c.119-2_131dup
NM_016346.4:c.119-2_131dup