Canonical Allele Identifier: CA1396728732

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119818444T= , CM000665.2:g.119818444T=	GRCh38
NC_000003.11:g.119537291T= , CM000665.1:g.119537291T=	GRCh37
NC_000003.10:g.121019981T=	NCBI36
NG_011856.1:g.42961T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.*1232T= MANE Select	ENSP00000377319.3:n.*1232T=
ENST00000466380.6:c.*1232T=	ENSP00000420297.2:n.*1232T=
ENST00000337940.4:c.*1232T=	ENSP00000336528.4:n.*1232T=
ENST00000393716.6:c.*1232T=	ENSP00000377319.2:n.*1232T=
ENST00000466380.5:c.*1232T=	ENSP00000420297.1:n.*1232T=
ENST00000493757.1:n.2669T=
NM_003889.3:c.*1232T=	NP_003880.3:n.*1232T=
NM_022002.2:c.*1232T=	NP_071285.1:n.*1232T=
NM_033013.2:c.*1232T=	NP_148934.1:n.*1232T=
NM_003889.4:c.*1232T= MANE Select	NP_003880.3:n.*1232T=
NM_022002.3:c.*1232T=	NP_071285.1:n.*1232T=
NM_033013.3:c.*1232T=	NP_148934.1:n.*1232T=