Canonical Allele Identifier: CA2629291434
Gene: NR2E3 HGNC NCBI

Linked Data

gnomAD v4: 15-71811388-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811388G>A , CM000677.2:g.71811388G>A GRCh38
NC_000015.9:g.72103728G>A , CM000677.1:g.72103728G>A GRCh37
NC_000015.8:g.69890782G>A NCBI36
NG_009113.2:g.5834G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.119-95G>A MANE Select ENSP00000482504.1:n.119-95G>A
ENST00000617575.4:c.119-95G>A ENSP00000482504.1:n.119-95G>A
ENST00000621098.1:c.119-95G>A ENSP00000479962.1:n.119-95G>A
ENST00000621736.4:c.-146-95G>A ENSP00000479254.1:n.-146-95G>A
NM_014249.3:c.119-95G>A NP_055064.1:n.119-95G>A
NM_016346.3:c.119-95G>A NP_057430.1:n.119-95G>A
XM_011521146.1:c.-146-95G>A XP_011519448.1:n.-146-95G>A
NM_014249.4:c.119-95G>A MANE Select NP_055064.1:n.119-95G>A
NM_016346.4:c.119-95G>A NP_057430.1:n.119-95G>A
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