Canonical Allele Identifier: CA2629291429
Gene: NR2E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811384G>T , CM000677.2:g.71811384G>T GRCh38
NC_000015.9:g.72103724G>T , CM000677.1:g.72103724G>T GRCh37
NC_000015.8:g.69890778G>T NCBI36
NG_009113.2:g.5830G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.119-99G>T MANE Select ENSP00000482504.1:n.119-99G>T
ENST00000617575.4:c.119-99G>T ENSP00000482504.1:n.119-99G>T
ENST00000621098.1:c.119-99G>T ENSP00000479962.1:n.119-99G>T
ENST00000621736.4:c.-146-99G>T ENSP00000479254.1:n.-146-99G>T
NM_014249.3:c.119-99G>T NP_055064.1:n.119-99G>T
NM_016346.3:c.119-99G>T NP_057430.1:n.119-99G>T
XM_011521146.1:c.-146-99G>T XP_011519448.1:n.-146-99G>T
NM_014249.4:c.119-99G>T MANE Select NP_055064.1:n.119-99G>T
NM_016346.4:c.119-99G>T NP_057430.1:n.119-99G>T