Canonical Allele Identifier: CA491103453
Gene: NR2E3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.72103824C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811484C>A , CM000677.2:g.71811484C>A GRCh38
NC_000015.9:g.72103824C>A , CM000677.1:g.72103824C>A GRCh37
NC_000015.8:g.69890878C>A NCBI36
NG_009113.2:g.5930C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.120C>A MANE Select ENSP00000482504.1:p.Gly40=
ENST00000617575.4:c.120C>A ENSP00000482504.1:p.Gly40=
ENST00000621098.1:c.120C>A ENSP00000479962.1:p.Gly40=
ENST00000621736.4:c.-145C>A ENSP00000479254.1:n.-145C>A
NM_014249.3:c.120C>A NP_055064.1:p.Gly40=
NM_016346.3:c.120C>A NP_057430.1:p.Gly40=
XM_011521146.1:c.-145C>A XP_011519448.1:n.-145C>A
NM_014249.4:c.120C>A MANE Select NP_055064.1:p.Gly40=
NM_016346.4:c.120C>A NP_057430.1:p.Gly40=