Canonical Allele Identifier: CA354055773
Gene: NR1I2 HGNC NCBI

Linked Data

dbSNP Id: rs377248798

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807347G>T , CM000665.2:g.119807347G>T GRCh38
NC_000003.11:g.119526194G>T , CM000665.1:g.119526194G>T GRCh37
NC_000003.10:g.121008884G>T NCBI36
NG_011856.1:g.31864G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393716.8:c.97G>T MANE Select ENSP00000377319.3:p.Glu33Ter
ENST00000466380.6:c.97G>T ENSP00000420297.2:p.Glu33Ter
ENST00000648112.1:c.*120G>T ENSP00000497876.1:n.*120G>T
ENST00000337940.4:c.214G>T ENSP00000336528.4:p.Glu72Ter
ENST00000393716.6:c.97G>T ENSP00000377319.2:p.Glu33Ter
ENST00000466380.5:c.97G>T ENSP00000420297.1:p.Glu33Ter
ENST00000474090.1:n.385G>T
NM_003889.3:c.97G>T NP_003880.3:p.Glu33Ter
NM_022002.2:c.214G>T NP_071285.1:p.Glu72Ter
NM_033013.2:c.97G>T NP_148934.1:p.Glu33Ter
NM_003889.4:c.97G>T MANE Select NP_003880.3:p.Glu33Ter
NM_022002.3:c.214G>T NP_071285.1:p.Glu72Ter
NM_033013.3:c.97G>T NP_148934.1:p.Glu33Ter