Canonical Allele Identifier: CA491103507

Gene: NR2E3

Linked Data

• MyVariant Identifiers: chr15:g.72103935G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811595G>C , CM000677.2:g.71811595G>C	GRCh38
NC_000015.9:g.72103935G>C , CM000677.1:g.72103935G>C	GRCh37
NC_000015.8:g.69890989G>C	NCBI36
NG_009113.2:g.6041G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.231G>C MANE Select	ENSP00000482504.1:p.Arg77=
ENST00000617575.4:c.231G>C	ENSP00000482504.1:p.Arg77=
ENST00000621098.1:c.231G>C	ENSP00000479962.1:p.Arg77=
ENST00000621736.4:c.-34G>C	ENSP00000479254.1:n.-34G>C
NM_014249.3:c.231G>C	NP_055064.1:p.Arg77=
NM_016346.3:c.231G>C	NP_057430.1:p.Arg77=
XM_011521146.1:c.-34G>C	XP_011519448.1:n.-34G>C
NM_014249.4:c.231G>C MANE Select	NP_055064.1:p.Arg77=
NM_016346.4:c.231G>C	NP_057430.1:p.Arg77=