Canonical Allele Identifier: CA492689925

Gene: NR2F2

Linked Data

• MyVariant Identifiers: chr15:g.96877807C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96334578C>T , CM000677.2:g.96334578C>T	GRCh38
NC_000015.9:g.96877807C>T , CM000677.1:g.96877807C>T	GRCh37
NC_000015.8:g.94678811C>T	NCBI36
NG_016753.1:g.13651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394166.8:c.945C>T MANE Select	ENSP00000377721.3:p.Leu315=
ENST00000394166.7:c.945C>T	ENSP00000377721.3:p.Leu315=
ENST00000394171.6:c.486C>T	ENSP00000377726.2:p.Leu162=
ENST00000421109.6:c.546C>T	ENSP00000401674.2:p.Leu182=
ENST00000453270.2:c.486C>T	ENSP00000389853.2:p.Leu162=
NM_001145155.1:c.546C>T	NP_001138627.1:p.Leu182=
NM_001145156.1:c.486C>T	NP_001138628.1:p.Leu162=
NM_001145157.1:c.486C>T	NP_001138629.1:p.Leu162=
NM_021005.3:c.945C>T	NP_066285.1:p.Leu315=
NM_021005.4:c.945C>T MANE Select	NP_066285.1:p.Leu315=
NM_001145155.2:c.546C>T	NP_001138627.1:p.Leu182=
NM_001145157.2:c.486C>T	NP_001138629.1:p.Leu162=