Canonical Allele Identifier: CA1396725559

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119811642G= , CM000665.2:g.119811642G=	GRCh38
NC_000003.11:g.119530489G= , CM000665.1:g.119530489G=	GRCh37
NC_000003.10:g.121013179G=	NCBI36
NG_011856.1:g.36159G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.435G= MANE Select	ENSP00000377319.3:p.Glu145=
ENST00000466380.6:c.435G=	ENSP00000420297.2:p.Glu145=
ENST00000337940.4:c.552G=	ENSP00000336528.4:p.Glu184=
ENST00000393716.6:c.435G=	ENSP00000377319.2:p.Glu145=
ENST00000466380.5:c.435G=	ENSP00000420297.1:p.Glu145=
ENST00000493757.1:n.567G=
NM_003889.3:c.435G=	NP_003880.3:p.Glu145=
NM_022002.2:c.552G=	NP_071285.1:p.Glu184=
NM_033013.2:c.435G=	NP_148934.1:p.Glu145=
NM_003889.4:c.435G= MANE Select	NP_003880.3:p.Glu145=
NM_022002.3:c.552G=	NP_071285.1:p.Glu184=
NM_033013.3:c.435G=	NP_148934.1:p.Glu145=