Canonical Allele Identifier: CA1396723502
Gene: NR1I2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807359G= , CM000665.2:g.119807359G= GRCh38
NC_000003.11:g.119526206G= , CM000665.1:g.119526206G= GRCh37
NC_000003.10:g.121008896G= NCBI36
NG_011856.1:g.31876G=

Transcript Alleles

HGVS Amino-acid change
ENST00000393716.8:c.109G= MANE Select ENSP00000377319.3:p.Gly37=
ENST00000466380.6:c.109G= ENSP00000420297.2:p.Gly37=
ENST00000648112.1:c.*132G= ENSP00000497876.1:n.*132G=
ENST00000337940.4:c.226G= ENSP00000336528.4:p.Gly76=
ENST00000393716.6:c.109G= ENSP00000377319.2:p.Gly37=
ENST00000466380.5:c.109G= ENSP00000420297.1:p.Gly37=
ENST00000474090.1:n.397G=
NM_003889.3:c.109G= NP_003880.3:p.Gly37=
NM_022002.2:c.226G= NP_071285.1:p.Gly76=
NM_033013.2:c.109G= NP_148934.1:p.Gly37=
NM_003889.4:c.109G= MANE Select NP_003880.3:p.Gly37=
NM_022002.3:c.226G= NP_071285.1:p.Gly76=
NM_033013.3:c.109G= NP_148934.1:p.Gly37=