Canonical Allele Identifier: CA1396723496
Gene: NR1I2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807349G= , CM000665.2:g.119807349G= GRCh38
NC_000003.11:g.119526196G= , CM000665.1:g.119526196G= GRCh37
NC_000003.10:g.121008886G= NCBI36
NG_011856.1:g.31866G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393716.8:c.99G= MANE Select ENSP00000377319.3:p.Glu33=
ENST00000466380.6:c.99G= ENSP00000420297.2:p.Glu33=
ENST00000648112.1:c.*122G= ENSP00000497876.1:n.*122G=
ENST00000337940.4:c.216G= ENSP00000336528.4:p.Glu72=
ENST00000393716.6:c.99G= ENSP00000377319.2:p.Glu33=
ENST00000466380.5:c.99G= ENSP00000420297.1:p.Glu33=
ENST00000474090.1:n.387G=
NM_003889.3:c.99G= NP_003880.3:p.Glu33=
NM_022002.2:c.216G= NP_071285.1:p.Glu72=
NM_033013.2:c.99G= NP_148934.1:p.Glu33=
NM_003889.4:c.99G= MANE Select NP_003880.3:p.Glu33=
NM_022002.3:c.216G= NP_071285.1:p.Glu72=
NM_033013.3:c.99G= NP_148934.1:p.Glu33=