Canonical Allele Identifier: CA1396723517

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807397T= , CM000665.2:g.119807397T=	GRCh38
NC_000003.11:g.119526244T= , CM000665.1:g.119526244T=	GRCh37
NC_000003.10:g.121008934T=	NCBI36
NG_011856.1:g.31914T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.147T= MANE Select	ENSP00000377319.3:p.Thr49=
ENST00000466380.6:c.147T=	ENSP00000420297.2:p.Thr49=
ENST00000648112.1:c.*170T=	ENSP00000497876.1:n.*170T=
ENST00000337940.4:c.264T=	ENSP00000336528.4:p.Thr88=
ENST00000393716.6:c.147T=	ENSP00000377319.2:p.Thr49=
ENST00000466380.5:c.147T=	ENSP00000420297.1:p.Thr49=
ENST00000474090.1:n.435T=
NM_003889.3:c.147T=	NP_003880.3:p.Thr49=
NM_022002.2:c.264T=	NP_071285.1:p.Thr88=
NM_033013.2:c.147T=	NP_148934.1:p.Thr49=
NM_003889.4:c.147T= MANE Select	NP_003880.3:p.Thr49=
NM_022002.3:c.264T=	NP_071285.1:p.Thr88=
NM_033013.3:c.147T=	NP_148934.1:p.Thr49=