Canonical Allele Identifier: CA393931550

Gene: NR2F2

Linked Data

• MyVariant Identifiers: chr15:g.96877815T>G (hg19) ; chr15:g.96334586T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96334586T>G , CM000677.2:g.96334586T>G	GRCh38
NC_000015.9:g.96877815T>G , CM000677.1:g.96877815T>G	GRCh37
NC_000015.8:g.94678819T>G	NCBI36
NG_016753.1:g.13659T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394166.8:c.953T>G MANE Select	ENSP00000377721.3:p.Ile318Arg
ENST00000394166.7:c.953T>G	ENSP00000377721.3:p.Ile318Arg
ENST00000394171.6:c.494T>G	ENSP00000377726.2:p.Ile165Arg
ENST00000421109.6:c.554T>G	ENSP00000401674.2:p.Ile185Arg
ENST00000453270.2:c.494T>G	ENSP00000389853.2:p.Ile165Arg
NM_001145155.1:c.554T>G	NP_001138627.1:p.Ile185Arg
NM_001145156.1:c.494T>G	NP_001138628.1:p.Ile165Arg
NM_001145157.1:c.494T>G	NP_001138629.1:p.Ile165Arg
NM_021005.3:c.953T>G	NP_066285.1:p.Ile318Arg
NM_021005.4:c.953T>G MANE Select	NP_066285.1:p.Ile318Arg
NM_001145155.2:c.554T>G	NP_001138627.1:p.Ile185Arg
NM_001145157.2:c.494T>G	NP_001138629.1:p.Ile165Arg