Canonical Allele Identifier: CA393032117

Gene: NR2E3

Linked Data

• dbSNP Id: rs2054180854
• gnomAD v3: 15-71811570-G-C
• gnomAD v4: 15-71811570-G-C
• MyVariant Identifiers: chr15:g.72103910G>C (hg19) ; chr15:g.71811570G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811570G>C , CM000677.2:g.71811570G>C	GRCh38
NC_000015.9:g.72103910G>C , CM000677.1:g.72103910G>C	GRCh37
NC_000015.8:g.69890964G>C	NCBI36
NG_009113.2:g.6016G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.206G>C MANE Select	ENSP00000482504.1:p.Gly69Ala
ENST00000617575.4:c.206G>C	ENSP00000482504.1:p.Gly69Ala
ENST00000621098.1:c.206G>C	ENSP00000479962.1:p.Gly69Ala
ENST00000621736.4:c.-59G>C	ENSP00000479254.1:n.-59G>C
NM_014249.3:c.206G>C	NP_055064.1:p.Gly69Ala
NM_016346.3:c.206G>C	NP_057430.1:p.Gly69Ala
XM_011521146.1:c.-59G>C	XP_011519448.1:n.-59G>C
NM_014249.4:c.206G>C MANE Select	NP_055064.1:p.Gly69Ala
NM_016346.4:c.206G>C	NP_057430.1:p.Gly69Ala