Canonical Allele Identifier: CA435219189

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526107A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807260A>C , CM000665.2:g.119807260A>C	GRCh38
NC_000003.11:g.119526107A>C , CM000665.1:g.119526107A>C	GRCh37
NC_000003.10:g.121008797A>C	NCBI36
NG_011856.1:g.31777A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393716.8:c.10A>C MANE Select	ENSP00000377319.3:p.Arg4=
ENST00000466380.6:c.10A>C	ENSP00000420297.2:p.Arg4=
ENST00000648112.1:c.*33A>C	ENSP00000497876.1:n.*33A>C
ENST00000337940.4:c.127A>C	ENSP00000336528.4:p.Arg43=
ENST00000393716.6:c.10A>C	ENSP00000377319.2:p.Arg4=
ENST00000466380.5:c.10A>C	ENSP00000420297.1:p.Arg4=
ENST00000474090.1:n.298A>C
NM_003889.3:c.10A>C	NP_003880.3:p.Arg4=
NM_022002.2:c.127A>C	NP_071285.1:p.Arg43=
NM_033013.2:c.10A>C	NP_148934.1:p.Arg4=
NM_003889.4:c.10A>C MANE Select	NP_003880.3:p.Arg4=
NM_022002.3:c.127A>C	NP_071285.1:p.Arg43=
NM_033013.3:c.10A>C	NP_148934.1:p.Arg4=