Canonical Allele Identifier: CA354055337

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526087C>A (hg19) ; chr3:g.119807240C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807240C>A , CM000665.2:g.119807240C>A	GRCh38
NC_000003.11:g.119526087C>A , CM000665.1:g.119526087C>A	GRCh37
NC_000003.10:g.121008777C>A	NCBI36
NG_011856.1:g.31757C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.-11C>A MANE Select	ENSP00000377319.3:n.-11C>A
ENST00000466380.6:c.-11C>A	ENSP00000420297.2:n.-11C>A
ENST00000648112.1:c.*13C>A	ENSP00000497876.1:n.*13C>A
ENST00000337940.4:c.107C>A	ENSP00000336528.4:p.Pro36Gln
ENST00000393716.6:c.-11C>A	ENSP00000377319.2:n.-11C>A
ENST00000466380.5:c.-11C>A	ENSP00000420297.1:n.-11C>A
ENST00000474090.1:n.278C>A
NM_003889.3:c.-11C>A	NP_003880.3:n.-11C>A
NM_022002.2:c.107C>A	NP_071285.1:p.Pro36Gln
NM_033013.2:c.-11C>A	NP_148934.1:n.-11C>A
NM_003889.4:c.-11C>A MANE Select	NP_003880.3:n.-11C>A
NM_022002.3:c.107C>A	NP_071285.1:p.Pro36Gln
NM_033013.3:c.-11C>A	NP_148934.1:n.-11C>A