Canonical Allele Identifier: CA1396728376

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119817650T= , CM000665.2:g.119817650T=	GRCh38
NC_000003.11:g.119536497T= , CM000665.1:g.119536497T=	GRCh37
NC_000003.10:g.121019187T=	NCBI36
NG_011856.1:g.42167T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000393716.8:c.*438T= MANE Select	ENSP00000377319.3:n.*438T=
ENST00000466380.6:c.*438T=	ENSP00000420297.2:n.*438T=
ENST00000337940.4:c.*438T=	ENSP00000336528.4:n.*438T=
ENST00000393716.6:c.*438T=	ENSP00000377319.2:n.*438T=
ENST00000466380.5:c.*438T=	ENSP00000420297.1:n.*438T=
ENST00000493757.1:n.1875T=
NM_003889.3:c.*438T=	NP_003880.3:n.*438T=
NM_022002.2:c.*438T=	NP_071285.1:n.*438T=
NM_033013.2:c.*438T=	NP_148934.1:n.*438T=
NM_003889.4:c.*438T= MANE Select	NP_003880.3:n.*438T=
NM_022002.3:c.*438T=	NP_071285.1:n.*438T=
NM_033013.3:c.*438T=	NP_148934.1:n.*438T=