Canonical Allele Identifier: CA2577909491
Gene: NR1I2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119811530T>A , CM000665.2:g.119811530T>A GRCh38
NC_000003.11:g.119530377T>A , CM000665.1:g.119530377T>A GRCh37
NC_000003.10:g.121013067T>A NCBI36
NG_011856.1:g.36047T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393716.8:c.332-9T>A MANE Select ENSP00000377319.3:n.332-9T>A
ENST00000466380.6:c.332-9T>A ENSP00000420297.2:n.332-9T>A
ENST00000337940.4:c.449-9T>A ENSP00000336528.4:n.449-9T>A
ENST00000393716.6:c.332-9T>A ENSP00000377319.2:n.332-9T>A
ENST00000466380.5:c.332-9T>A ENSP00000420297.1:n.332-9T>A
ENST00000493757.1:n.455T>A
NM_003889.3:c.332-9T>A NP_003880.3:n.332-9T>A
NM_022002.2:c.449-9T>A NP_071285.1:n.449-9T>A
NM_033013.2:c.332-9T>A NP_148934.1:n.332-9T>A
NM_003889.4:c.332-9T>A MANE Select NP_003880.3:n.332-9T>A
NM_022002.3:c.449-9T>A NP_071285.1:n.449-9T>A
NM_033013.3:c.332-9T>A NP_148934.1:n.332-9T>A