Canonical Allele Identifier: CA1396723587

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807568C= , CM000665.2:g.119807568C=	GRCh38
NC_000003.11:g.119526415C= , CM000665.1:g.119526415C=	GRCh37
NC_000003.10:g.121009105C=	NCBI36
NG_011856.1:g.32085C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.197+121C= MANE Select	ENSP00000377319.3:n.197+121C=
ENST00000466380.6:c.197+121C=	ENSP00000420297.2:n.197+121C=
ENST00000648112.1:c.*341C=	ENSP00000497876.1:n.*341C=
ENST00000337940.4:c.314+121C=	ENSP00000336528.4:n.314+121C=
ENST00000393716.6:c.197+121C=	ENSP00000377319.2:n.197+121C=
ENST00000466380.5:c.197+121C=	ENSP00000420297.1:n.197+121C=
ENST00000474090.1:n.485+121C=
NM_003889.3:c.197+121C=	NP_003880.3:n.197+121C=
NM_022002.2:c.314+121C=	NP_071285.1:n.314+121C=
NM_033013.2:c.197+121C=	NP_148934.1:n.197+121C=
NM_003889.4:c.197+121C= MANE Select	NP_003880.3:n.197+121C=
NM_022002.3:c.314+121C=	NP_071285.1:n.314+121C=
NM_033013.3:c.197+121C=	NP_148934.1:n.197+121C=