Canonical Allele Identifier: CA1396728487

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119817871C= , CM000665.2:g.119817871C=	GRCh38
NC_000003.11:g.119536718C= , CM000665.1:g.119536718C=	GRCh37
NC_000003.10:g.121019408C=	NCBI36
NG_011856.1:g.42388C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.*659C= MANE Select	ENSP00000377319.3:n.*659C=
ENST00000466380.6:c.*659C=	ENSP00000420297.2:n.*659C=
ENST00000337940.4:c.*659C=	ENSP00000336528.4:n.*659C=
ENST00000393716.6:c.*659C=	ENSP00000377319.2:n.*659C=
ENST00000466380.5:c.*659C=	ENSP00000420297.1:n.*659C=
ENST00000493757.1:n.2096C=
NM_003889.3:c.*659C=	NP_003880.3:n.*659C=
NM_022002.2:c.*659C=	NP_071285.1:n.*659C=
NM_033013.2:c.*659C=	NP_148934.1:n.*659C=
NM_003889.4:c.*659C= MANE Select	NP_003880.3:n.*659C=
NM_022002.3:c.*659C=	NP_071285.1:n.*659C=
NM_033013.3:c.*659C=	NP_148934.1:n.*659C=