Canonical Allele Identifier: CA2186513485
Gene: NR2E3 HGNC NCBI

Linked Data

dbSNP Id: rs955454233

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811400A>G , CM000677.2:g.71811400A>G GRCh38
NC_000015.9:g.72103740A>G , CM000677.1:g.72103740A>G GRCh37
NC_000015.8:g.69890794A>G NCBI36
NG_009113.2:g.5846A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.119-83A>G MANE Select ENSP00000482504.1:n.119-83A>G
ENST00000617575.4:c.119-83A>G ENSP00000482504.1:n.119-83A>G
ENST00000621098.1:c.119-83A>G ENSP00000479962.1:n.119-83A>G
ENST00000621736.4:c.-146-83A>G ENSP00000479254.1:n.-146-83A>G
NM_014249.3:c.119-83A>G NP_055064.1:n.119-83A>G
NM_016346.3:c.119-83A>G NP_057430.1:n.119-83A>G
XM_011521146.1:c.-146-83A>G XP_011519448.1:n.-146-83A>G
NM_014249.4:c.119-83A>G MANE Select NP_055064.1:n.119-83A>G
NM_016346.4:c.119-83A>G NP_057430.1:n.119-83A>G