Canonical Allele Identifier: CA492689939

Gene: NR2F2

Linked Data

• MyVariant Identifiers: chr15:g.96877816A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96334587A>T , CM000677.2:g.96334587A>T	GRCh38
NC_000015.9:g.96877816A>T , CM000677.1:g.96877816A>T	GRCh37
NC_000015.8:g.94678820A>T	NCBI36
NG_016753.1:g.13660A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394166.8:c.954A>T MANE Select	ENSP00000377721.3:p.Ile318=
ENST00000394166.7:c.954A>T	ENSP00000377721.3:p.Ile318=
ENST00000394171.6:c.495A>T	ENSP00000377726.2:p.Ile165=
ENST00000421109.6:c.555A>T	ENSP00000401674.2:p.Ile185=
ENST00000453270.2:c.495A>T	ENSP00000389853.2:p.Ile165=
NM_001145155.1:c.555A>T	NP_001138627.1:p.Ile185=
NM_001145156.1:c.495A>T	NP_001138628.1:p.Ile165=
NM_001145157.1:c.495A>T	NP_001138629.1:p.Ile165=
NM_021005.3:c.954A>T	NP_066285.1:p.Ile318=
NM_021005.4:c.954A>T MANE Select	NP_066285.1:p.Ile318=
NM_001145155.2:c.555A>T	NP_001138627.1:p.Ile185=
NM_001145157.2:c.495A>T	NP_001138629.1:p.Ile165=