Canonical Allele Identifier: CA354058278

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119530494A>C (hg19) ; chr3:g.119811647A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119811647A>C , CM000665.2:g.119811647A>C	GRCh38
NC_000003.11:g.119530494A>C , CM000665.1:g.119530494A>C	GRCh37
NC_000003.10:g.121013184A>C	NCBI36
NG_011856.1:g.36164A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.440A>C MANE Select	ENSP00000377319.3:p.Gln147Pro
ENST00000466380.6:c.440A>C	ENSP00000420297.2:p.Gln147Pro
ENST00000337940.4:c.557A>C	ENSP00000336528.4:p.Gln186Pro
ENST00000393716.6:c.440A>C	ENSP00000377319.2:p.Gln147Pro
ENST00000466380.5:c.440A>C	ENSP00000420297.1:p.Gln147Pro
ENST00000493757.1:n.572A>C
NM_003889.3:c.440A>C	NP_003880.3:p.Gln147Pro
NM_022002.2:c.557A>C	NP_071285.1:p.Gln186Pro
NM_033013.2:c.440A>C	NP_148934.1:p.Gln147Pro
NM_003889.4:c.440A>C MANE Select	NP_003880.3:p.Gln147Pro
NM_022002.3:c.557A>C	NP_071285.1:p.Gln186Pro
NM_033013.3:c.440A>C	NP_148934.1:p.Gln147Pro