Canonical Allele Identifier: CA1396723546

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807451G= , CM000665.2:g.119807451G=	GRCh38
NC_000003.11:g.119526298G= , CM000665.1:g.119526298G=	GRCh37
NC_000003.10:g.121008988G=	NCBI36
NG_011856.1:g.31968G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.197+4G= MANE Select	ENSP00000377319.3:n.197+4G=
ENST00000466380.6:c.197+4G=	ENSP00000420297.2:n.197+4G=
ENST00000648112.1:c.*224G=	ENSP00000497876.1:n.*224G=
ENST00000337940.4:c.314+4G=	ENSP00000336528.4:n.314+4G=
ENST00000393716.6:c.197+4G=	ENSP00000377319.2:n.197+4G=
ENST00000466380.5:c.197+4G=	ENSP00000420297.1:n.197+4G=
ENST00000474090.1:n.485+4G=
NM_003889.3:c.197+4G=	NP_003880.3:n.197+4G=
NM_022002.2:c.314+4G=	NP_071285.1:n.314+4G=
NM_033013.2:c.197+4G=	NP_148934.1:n.197+4G=
NM_003889.4:c.197+4G= MANE Select	NP_003880.3:n.197+4G=
NM_022002.3:c.314+4G=	NP_071285.1:n.314+4G=
NM_033013.3:c.197+4G=	NP_148934.1:n.197+4G=