Canonical Allele Identifier: CA393930761

Gene: NR2F2

Linked Data

• ClinVar Variation Id: 1452069
• ClinVar RCV Id: RCV001994474
• dbSNP Id: rs2141169116
• MyVariant Identifiers: chr15:g.96877466C>T (hg19) ; chr15:g.96334237C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96334237C>T , CM000677.2:g.96334237C>T	GRCh38
NC_000015.9:g.96877466C>T , CM000677.1:g.96877466C>T	GRCh37
NC_000015.8:g.94678470C>T	NCBI36
NG_016753.1:g.13310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394166.8:c.604C>T MANE Select	ENSP00000377721.3:p.Gln202Ter
ENST00000394166.7:c.604C>T	ENSP00000377721.3:p.Gln202Ter
ENST00000394171.6:c.145C>T	ENSP00000377726.2:p.Gln49Ter
ENST00000421109.6:c.205C>T	ENSP00000401674.2:p.Gln69Ter
ENST00000453270.2:c.145C>T	ENSP00000389853.2:p.Gln49Ter
ENST00000559679.1:c.145C>T	ENSP00000457112.1:p.Gln49Ter
NM_001145155.1:c.205C>T	NP_001138627.1:p.Gln69Ter
NM_001145156.1:c.145C>T	NP_001138628.1:p.Gln49Ter
NM_001145157.1:c.145C>T	NP_001138629.1:p.Gln49Ter
NM_021005.3:c.604C>T	NP_066285.1:p.Gln202Ter
NM_021005.4:c.604C>T MANE Select	NP_066285.1:p.Gln202Ter
NM_001145155.2:c.205C>T	NP_001138627.1:p.Gln69Ter
NM_001145157.2:c.145C>T	NP_001138629.1:p.Gln49Ter