Canonical Allele Identifier: CA354056014
Gene: NR1I2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807417T>A , CM000665.2:g.119807417T>A GRCh38
NC_000003.11:g.119526264T>A , CM000665.1:g.119526264T>A GRCh37
NC_000003.10:g.121008954T>A NCBI36
NG_011856.1:g.31934T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393716.8:c.167T>A MANE Select ENSP00000377319.3:p.Met56Lys
ENST00000466380.6:c.167T>A ENSP00000420297.2:p.Met56Lys
ENST00000648112.1:c.*190T>A ENSP00000497876.1:n.*190T>A
ENST00000337940.4:c.284T>A ENSP00000336528.4:p.Met95Lys
ENST00000393716.6:c.167T>A ENSP00000377319.2:p.Met56Lys
ENST00000466380.5:c.167T>A ENSP00000420297.1:p.Met56Lys
ENST00000474090.1:n.455T>A
NM_003889.3:c.167T>A NP_003880.3:p.Met56Lys
NM_022002.2:c.284T>A NP_071285.1:p.Met95Lys
NM_033013.2:c.167T>A NP_148934.1:p.Met56Lys
NM_003889.4:c.167T>A MANE Select NP_003880.3:p.Met56Lys
NM_022002.3:c.284T>A NP_071285.1:p.Met95Lys
NM_033013.3:c.167T>A NP_148934.1:p.Met56Lys