Canonical Allele Identifier: CA393931526

Gene: NR2F2

Linked Data

• MyVariant Identifiers: chr15:g.96877805C>T (hg19) ; chr15:g.96334576C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96334576C>T , CM000677.2:g.96334576C>T	GRCh38
NC_000015.9:g.96877805C>T , CM000677.1:g.96877805C>T	GRCh37
NC_000015.8:g.94678809C>T	NCBI36
NG_016753.1:g.13649C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394166.8:c.943C>T MANE Select	ENSP00000377721.3:p.Leu315Phe
ENST00000394166.7:c.943C>T	ENSP00000377721.3:p.Leu315Phe
ENST00000394171.6:c.484C>T	ENSP00000377726.2:p.Leu162Phe
ENST00000421109.6:c.544C>T	ENSP00000401674.2:p.Leu182Phe
ENST00000453270.2:c.484C>T	ENSP00000389853.2:p.Leu162Phe
NM_001145155.1:c.544C>T	NP_001138627.1:p.Leu182Phe
NM_001145156.1:c.484C>T	NP_001138628.1:p.Leu162Phe
NM_001145157.1:c.484C>T	NP_001138629.1:p.Leu162Phe
NM_021005.3:c.943C>T	NP_066285.1:p.Leu315Phe
NM_021005.4:c.943C>T MANE Select	NP_066285.1:p.Leu315Phe
NM_001145155.2:c.544C>T	NP_001138627.1:p.Leu182Phe
NM_001145157.2:c.484C>T	NP_001138629.1:p.Leu162Phe