Canonical Allele Identifier: CA1396723457
Gene: NR1I2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807266A= , CM000665.2:g.119807266A= GRCh38
NC_000003.11:g.119526113A= , CM000665.1:g.119526113A= GRCh37
NC_000003.10:g.121008803A= NCBI36
NG_011856.1:g.31783A=

Transcript Alleles

HGVS Amino-acid change
ENST00000393716.8:c.16A= MANE Select ENSP00000377319.3:p.Lys6=
ENST00000466380.6:c.16A= ENSP00000420297.2:p.Lys6=
ENST00000648112.1:c.*39A= ENSP00000497876.1:n.*39A=
ENST00000337940.4:c.133A= ENSP00000336528.4:p.Lys45=
ENST00000393716.6:c.16A= ENSP00000377319.2:p.Lys6=
ENST00000466380.5:c.16A= ENSP00000420297.1:p.Lys6=
ENST00000474090.1:n.304A=
NM_003889.3:c.16A= NP_003880.3:p.Lys6=
NM_022002.2:c.133A= NP_071285.1:p.Lys45=
NM_033013.2:c.16A= NP_148934.1:p.Lys6=
NM_003889.4:c.16A= MANE Select NP_003880.3:p.Lys6=
NM_022002.3:c.133A= NP_071285.1:p.Lys45=
NM_033013.3:c.16A= NP_148934.1:p.Lys6=