Canonical Allele Identifier: CA1396728429
Gene: NR1I2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119817737A= , CM000665.2:g.119817737A= GRCh38
NC_000003.11:g.119536584A= , CM000665.1:g.119536584A= GRCh37
NC_000003.10:g.121019274A= NCBI36
NG_011856.1:g.42254A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393716.8:c.*525A= MANE Select ENSP00000377319.3:n.*525A=
ENST00000466380.6:c.*525A= ENSP00000420297.2:n.*525A=
ENST00000337940.4:c.*525A= ENSP00000336528.4:n.*525A=
ENST00000393716.6:c.*525A= ENSP00000377319.2:n.*525A=
ENST00000466380.5:c.*525A= ENSP00000420297.1:n.*525A=
ENST00000493757.1:n.1962A=
NM_003889.3:c.*525A= NP_003880.3:n.*525A=
NM_022002.2:c.*525A= NP_071285.1:n.*525A=
NM_033013.2:c.*525A= NP_148934.1:n.*525A=
NM_003889.4:c.*525A= MANE Select NP_003880.3:n.*525A=
NM_022002.3:c.*525A= NP_071285.1:n.*525A=
NM_033013.3:c.*525A= NP_148934.1:n.*525A=