Canonical Allele Identifier: CA1396723487

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807333G= , CM000665.2:g.119807333G=	GRCh38
NC_000003.11:g.119526180G= , CM000665.1:g.119526180G=	GRCh37
NC_000003.10:g.121008870G=	NCBI36
NG_011856.1:g.31850G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.83G= MANE Select	ENSP00000377319.3:p.Ser28=
ENST00000466380.6:c.83G=	ENSP00000420297.2:p.Ser28=
ENST00000648112.1:c.*106G=	ENSP00000497876.1:n.*106G=
ENST00000337940.4:c.200G=	ENSP00000336528.4:p.Ser67=
ENST00000393716.6:c.83G=	ENSP00000377319.2:p.Ser28=
ENST00000466380.5:c.83G=	ENSP00000420297.1:p.Ser28=
ENST00000474090.1:n.371G=
NM_003889.3:c.83G=	NP_003880.3:p.Ser28=
NM_022002.2:c.200G=	NP_071285.1:p.Ser67=
NM_033013.2:c.83G=	NP_148934.1:p.Ser28=
NM_003889.4:c.83G= MANE Select	NP_003880.3:p.Ser28=
NM_022002.3:c.200G=	NP_071285.1:p.Ser67=
NM_033013.3:c.83G=	NP_148934.1:p.Ser28=