Canonical Allele Identifier: CA354057535

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119530384A>C (hg19) ; chr3:g.119811537A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119811537A>C , CM000665.2:g.119811537A>C	GRCh38
NC_000003.11:g.119530384A>C , CM000665.1:g.119530384A>C	GRCh37
NC_000003.10:g.121013074A>C	NCBI36
NG_011856.1:g.36054A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.332-2A>C MANE Select	ENSP00000377319.3:n.332-2A>C
ENST00000466380.6:c.332-2A>C	ENSP00000420297.2:n.332-2A>C
ENST00000337940.4:c.449-2A>C	ENSP00000336528.4:n.449-2A>C
ENST00000393716.6:c.332-2A>C	ENSP00000377319.2:n.332-2A>C
ENST00000466380.5:c.332-2A>C	ENSP00000420297.1:n.332-2A>C
ENST00000493757.1:n.462A>C
NM_003889.3:c.332-2A>C	NP_003880.3:n.332-2A>C
NM_022002.2:c.449-2A>C	NP_071285.1:n.449-2A>C
NM_033013.2:c.332-2A>C	NP_148934.1:n.332-2A>C
NM_003889.4:c.332-2A>C MANE Select	NP_003880.3:n.332-2A>C
NM_022002.3:c.449-2A>C	NP_071285.1:n.449-2A>C
NM_033013.3:c.332-2A>C	NP_148934.1:n.332-2A>C