Canonical Allele Identifier: CA435220198

Gene: NR1I2

Linked Data

• dbSNP Id: rs1577284623
• MyVariant Identifiers: chr3:g.119530486A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119811639A>C , CM000665.2:g.119811639A>C	GRCh38
NC_000003.11:g.119530486A>C , CM000665.1:g.119530486A>C	GRCh37
NC_000003.10:g.121013176A>C	NCBI36
NG_011856.1:g.36156A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.432A>C MANE Select	ENSP00000377319.3:p.Thr144=
ENST00000466380.6:c.432A>C	ENSP00000420297.2:p.Thr144=
ENST00000337940.4:c.549A>C	ENSP00000336528.4:p.Thr183=
ENST00000393716.6:c.432A>C	ENSP00000377319.2:p.Thr144=
ENST00000466380.5:c.432A>C	ENSP00000420297.1:p.Thr144=
ENST00000493757.1:n.564A>C
NM_003889.3:c.432A>C	NP_003880.3:p.Thr144=
NM_022002.2:c.549A>C	NP_071285.1:p.Thr183=
NM_033013.2:c.432A>C	NP_148934.1:p.Thr144=
NM_003889.4:c.432A>C MANE Select	NP_003880.3:p.Thr144=
NM_022002.3:c.549A>C	NP_071285.1:p.Thr183=
NM_033013.3:c.432A>C	NP_148934.1:p.Thr144=