Canonical Allele Identifier: CA393032161
Gene: NR2E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811590C>G , CM000677.2:g.71811590C>G GRCh38
NC_000015.9:g.72103930C>G , CM000677.1:g.72103930C>G GRCh37
NC_000015.8:g.69890984C>G NCBI36
NG_009113.2:g.6036C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.226C>G MANE Select ENSP00000482504.1:p.Arg76Gly
ENST00000617575.4:c.226C>G ENSP00000482504.1:p.Arg76Gly
ENST00000621098.1:c.226C>G ENSP00000479962.1:p.Arg76Gly
ENST00000621736.4:c.-39C>G ENSP00000479254.1:n.-39C>G
NM_014249.3:c.226C>G NP_055064.1:p.Arg76Gly
NM_016346.3:c.226C>G NP_057430.1:p.Arg76Gly
XM_011521146.1:c.-39C>G XP_011519448.1:n.-39C>G
NM_014249.4:c.226C>G MANE Select NP_055064.1:p.Arg76Gly
NM_016346.4:c.226C>G NP_057430.1:p.Arg76Gly