Canonical Allele Identifier: CA393032073

Gene: NR2E3

Linked Data

• MyVariant Identifiers: chr15:g.72103890T>G (hg19) ; chr15:g.71811550T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811550T>G , CM000677.2:g.71811550T>G	GRCh38
NC_000015.9:g.72103890T>G , CM000677.1:g.72103890T>G	GRCh37
NC_000015.8:g.69890944T>G	NCBI36
NG_009113.2:g.5996T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.186T>G MANE Select	ENSP00000482504.1:p.Tyr62Ter
ENST00000617575.4:c.186T>G	ENSP00000482504.1:p.Tyr62Ter
ENST00000621098.1:c.186T>G	ENSP00000479962.1:p.Tyr62Ter
ENST00000621736.4:c.-79T>G	ENSP00000479254.1:n.-79T>G
NM_014249.3:c.186T>G	NP_055064.1:p.Tyr62Ter
NM_016346.3:c.186T>G	NP_057430.1:p.Tyr62Ter
XM_011521146.1:c.-79T>G	XP_011519448.1:n.-79T>G
NM_014249.4:c.186T>G MANE Select	NP_055064.1:p.Tyr62Ter
NM_016346.4:c.186T>G	NP_057430.1:p.Tyr62Ter