Canonical Allele Identifier: CA1396723529

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807419A= , CM000665.2:g.119807419A=	GRCh38
NC_000003.11:g.119526266A= , CM000665.1:g.119526266A=	GRCh37
NC_000003.10:g.121008956A=	NCBI36
NG_011856.1:g.31936A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.169A= MANE Select	ENSP00000377319.3:p.Thr57=
ENST00000466380.6:c.169A=	ENSP00000420297.2:p.Thr57=
ENST00000648112.1:c.*192A=	ENSP00000497876.1:n.*192A=
ENST00000337940.4:c.286A=	ENSP00000336528.4:p.Thr96=
ENST00000393716.6:c.169A=	ENSP00000377319.2:p.Thr57=
ENST00000466380.5:c.169A=	ENSP00000420297.1:p.Thr57=
ENST00000474090.1:n.457A=
NM_003889.3:c.169A=	NP_003880.3:p.Thr57=
NM_022002.2:c.286A=	NP_071285.1:p.Thr96=
NM_033013.2:c.169A=	NP_148934.1:p.Thr57=
NM_003889.4:c.169A= MANE Select	NP_003880.3:p.Thr57=
NM_022002.3:c.286A=	NP_071285.1:p.Thr96=
NM_033013.3:c.169A=	NP_148934.1:p.Thr57=