Canonical Allele Identifier: CA1396723442

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807232A= , CM000665.2:g.119807232A=	GRCh38
NC_000003.11:g.119526079A= , CM000665.1:g.119526079A=	GRCh37
NC_000003.10:g.121008769A=	NCBI36
NG_011856.1:g.31749A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.-19A= MANE Select	ENSP00000377319.3:n.-19A=
ENST00000466380.6:c.-19A=	ENSP00000420297.2:n.-19A=
ENST00000648112.1:c.*5A=	ENSP00000497876.1:n.*5A=
ENST00000337940.4:c.99A=	ENSP00000336528.4:p.Pro33=
ENST00000393716.6:c.-19A=	ENSP00000377319.2:n.-19A=
ENST00000466380.5:c.-19A=	ENSP00000420297.1:n.-19A=
ENST00000474090.1:n.270A=
NM_003889.3:c.-19A=	NP_003880.3:n.-19A=
NM_022002.2:c.99A=	NP_071285.1:p.Pro33=
NM_033013.2:c.-19A=	NP_148934.1:n.-19A=
NM_003889.4:c.-19A= MANE Select	NP_003880.3:n.-19A=
NM_022002.3:c.99A=	NP_071285.1:p.Pro33=
NM_033013.3:c.-19A=	NP_148934.1:n.-19A=