Canonical Allele Identifier: CA1396712468

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119783284A= , CM000665.2:g.119783284A=	GRCh38
NC_000003.11:g.119502131A= , CM000665.1:g.119502131A=	GRCh37
NC_000003.10:g.120984821A=	NCBI36
NG_011856.1:g.7801A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000393716.8:c.-23+984A= MANE Select	ENSP00000377319.3:n.-23+984A=
ENST00000466380.6:c.-23+984A=	ENSP00000420297.2:n.-23+984A=
ENST00000648112.1:c.*2-23945A=	ENSP00000497876.1:n.*2-23945A=
ENST00000337940.4:c.95+432A=	ENSP00000336528.4:n.95+432A=
ENST00000393716.6:c.-23+984A=	ENSP00000377319.2:n.-23+984A=
ENST00000466380.5:c.-23+984A=	ENSP00000420297.1:n.-23+984A=
ENST00000474090.1:n.266+984A=
NM_003889.3:c.-23+984A=	NP_003880.3:n.-23+984A=
NM_022002.2:c.95+432A=	NP_071285.1:n.95+432A=
NM_033013.2:c.-23+984A=	NP_148934.1:n.-23+984A=
NM_003889.4:c.-23+984A= MANE Select	NP_003880.3:n.-23+984A=
NM_022002.3:c.95+432A=	NP_071285.1:n.95+432A=
NM_033013.3:c.-23+984A=	NP_148934.1:n.-23+984A=