Canonical Allele Identifier: CA2629291419

Gene: NR2E3

Linked Data

• gnomAD v4: 15-71811376-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811376T>C , CM000677.2:g.71811376T>C	GRCh38
NC_000015.9:g.72103716T>C , CM000677.1:g.72103716T>C	GRCh37
NC_000015.8:g.69890770T>C	NCBI36
NG_009113.2:g.5822T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.119-107T>C MANE Select	ENSP00000482504.1:n.119-107T>C
ENST00000617575.4:c.119-107T>C	ENSP00000482504.1:n.119-107T>C
ENST00000621098.1:c.119-107T>C	ENSP00000479962.1:n.119-107T>C
ENST00000621736.4:c.-146-107T>C	ENSP00000479254.1:n.-146-107T>C
NM_014249.3:c.119-107T>C	NP_055064.1:n.119-107T>C
NM_016346.3:c.119-107T>C	NP_057430.1:n.119-107T>C
XM_011521146.1:c.-146-107T>C	XP_011519448.1:n.-146-107T>C
NM_014249.4:c.119-107T>C MANE Select	NP_055064.1:n.119-107T>C
NM_016346.4:c.119-107T>C	NP_057430.1:n.119-107T>C