Canonical Allele Identifier: CA1396725503

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119811541A= , CM000665.2:g.119811541A=	GRCh38
NC_000003.11:g.119530388A= , CM000665.1:g.119530388A=	GRCh37
NC_000003.10:g.121013078A=	NCBI36
NG_011856.1:g.36058A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.334A= MANE Select	ENSP00000377319.3:p.Ile112=
ENST00000466380.6:c.334A=	ENSP00000420297.2:p.Ile112=
ENST00000337940.4:c.451A=	ENSP00000336528.4:p.Ile151=
ENST00000393716.6:c.334A=	ENSP00000377319.2:p.Ile112=
ENST00000466380.5:c.334A=	ENSP00000420297.1:p.Ile112=
ENST00000493757.1:n.466A=
NM_003889.3:c.334A=	NP_003880.3:p.Ile112=
NM_022002.2:c.451A=	NP_071285.1:p.Ile151=
NM_033013.2:c.334A=	NP_148934.1:p.Ile112=
NM_003889.4:c.334A= MANE Select	NP_003880.3:p.Ile112=
NM_022002.3:c.451A=	NP_071285.1:p.Ile151=
NM_033013.3:c.334A=	NP_148934.1:p.Ile112=