Canonical Allele Identifier: CA2186513554
Gene: NR2E3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811485G= , CM000677.2:g.71811485G= GRCh38
NC_000015.9:g.72103825G= , CM000677.1:g.72103825G= GRCh37
NC_000015.8:g.69890879G= NCBI36
NG_009113.2:g.5931G=

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.121G= MANE Select ENSP00000482504.1:p.Val41=
ENST00000617575.4:c.121G= ENSP00000482504.1:p.Val41=
ENST00000621098.1:c.121G= ENSP00000479962.1:p.Val41=
ENST00000621736.4:c.-144G= ENSP00000479254.1:n.-144G=
NM_014249.3:c.121G= NP_055064.1:p.Val41=
NM_016346.3:c.121G= NP_057430.1:p.Val41=
XM_011521146.1:c.-144G= XP_011519448.1:n.-144G=
NM_014249.4:c.121G= MANE Select NP_055064.1:p.Val41=
NM_016346.4:c.121G= NP_057430.1:p.Val41=