Canonical Allele Identifier: CA1396723519

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807399G= , CM000665.2:g.119807399G=	GRCh38
NC_000003.11:g.119526246G= , CM000665.1:g.119526246G=	GRCh37
NC_000003.10:g.121008936G=	NCBI36
NG_011856.1:g.31916G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.149G= MANE Select	ENSP00000377319.3:p.Gly50=
ENST00000466380.6:c.149G=	ENSP00000420297.2:p.Gly50=
ENST00000648112.1:c.*172G=	ENSP00000497876.1:n.*172G=
ENST00000337940.4:c.266G=	ENSP00000336528.4:p.Gly89=
ENST00000393716.6:c.149G=	ENSP00000377319.2:p.Gly50=
ENST00000466380.5:c.149G=	ENSP00000420297.1:p.Gly50=
ENST00000474090.1:n.437G=
NM_003889.3:c.149G=	NP_003880.3:p.Gly50=
NM_022002.2:c.266G=	NP_071285.1:p.Gly89=
NM_033013.2:c.149G=	NP_148934.1:p.Gly50=
NM_003889.4:c.149G= MANE Select	NP_003880.3:p.Gly50=
NM_022002.3:c.266G=	NP_071285.1:p.Gly89=
NM_033013.3:c.149G=	NP_148934.1:p.Gly50=