Canonical Allele Identifier: CA393931522

Gene: NR2F2

Linked Data

• MyVariant Identifiers: chr15:g.96877803G>C (hg19) ; chr15:g.96334574G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96334574G>C , CM000677.2:g.96334574G>C	GRCh38
NC_000015.9:g.96877803G>C , CM000677.1:g.96877803G>C	GRCh37
NC_000015.8:g.94678807G>C	NCBI36
NG_016753.1:g.13647G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394166.8:c.941G>C MANE Select	ENSP00000377721.3:p.Cys314Ser
ENST00000394166.7:c.941G>C	ENSP00000377721.3:p.Cys314Ser
ENST00000394171.6:c.482G>C	ENSP00000377726.2:p.Cys161Ser
ENST00000421109.6:c.542G>C	ENSP00000401674.2:p.Cys181Ser
ENST00000453270.2:c.482G>C	ENSP00000389853.2:p.Cys161Ser
NM_001145155.1:c.542G>C	NP_001138627.1:p.Cys181Ser
NM_001145156.1:c.482G>C	NP_001138628.1:p.Cys161Ser
NM_001145157.1:c.482G>C	NP_001138629.1:p.Cys161Ser
NM_021005.3:c.941G>C	NP_066285.1:p.Cys314Ser
NM_021005.4:c.941G>C MANE Select	NP_066285.1:p.Cys314Ser
NM_001145155.2:c.542G>C	NP_001138627.1:p.Cys181Ser
NM_001145157.2:c.482G>C	NP_001138629.1:p.Cys161Ser