Canonical Allele Identifier: CA354055775
Gene: NR1I2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807348A>C , CM000665.2:g.119807348A>C GRCh38
NC_000003.11:g.119526195A>C , CM000665.1:g.119526195A>C GRCh37
NC_000003.10:g.121008885A>C NCBI36
NG_011856.1:g.31865A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393716.8:c.98A>C MANE Select ENSP00000377319.3:p.Glu33Ala
ENST00000466380.6:c.98A>C ENSP00000420297.2:p.Glu33Ala
ENST00000648112.1:c.*121A>C ENSP00000497876.1:n.*121A>C
ENST00000337940.4:c.215A>C ENSP00000336528.4:p.Glu72Ala
ENST00000393716.6:c.98A>C ENSP00000377319.2:p.Glu33Ala
ENST00000466380.5:c.98A>C ENSP00000420297.1:p.Glu33Ala
ENST00000474090.1:n.386A>C
NM_003889.3:c.98A>C NP_003880.3:p.Glu33Ala
NM_022002.2:c.215A>C NP_071285.1:p.Glu72Ala
NM_033013.2:c.98A>C NP_148934.1:p.Glu33Ala
NM_003889.4:c.98A>C MANE Select NP_003880.3:p.Glu33Ala
NM_022002.3:c.215A>C NP_071285.1:p.Glu72Ala
NM_033013.3:c.98A>C NP_148934.1:p.Glu33Ala