Canonical Allele Identifier: CA2629291619

Gene: NR2E3

Linked Data

• gnomAD v4: 15-71811699-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811699A>G , CM000677.2:g.71811699A>G	GRCh38
NC_000015.9:g.72104039A>G , CM000677.1:g.72104039A>G	GRCh37
NC_000015.8:g.69891093A>G	NCBI36
NG_009113.2:g.6145A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.246-67A>G MANE Select	ENSP00000482504.1:n.246-67A>G
ENST00000617575.4:c.246-67A>G	ENSP00000482504.1:n.246-67A>G
ENST00000621098.1:c.246-67A>G	ENSP00000479962.1:n.246-67A>G
ENST00000621736.4:c.-19-67A>G	ENSP00000479254.1:n.-19-67A>G
NM_014249.3:c.246-67A>G	NP_055064.1:n.246-67A>G
NM_016346.3:c.246-67A>G	NP_057430.1:n.246-67A>G
XM_011521146.1:c.-19-67A>G	XP_011519448.1:n.-19-67A>G
NM_014249.4:c.246-67A>G MANE Select	NP_055064.1:n.246-67A>G
NM_016346.4:c.246-67A>G	NP_057430.1:n.246-67A>G